Open, ClassifiedPosted Jan 15, 2026·Initiated Dec 12, 2025
ThinPrep CytoLyt Solution. Buffered Cell Wash Solution.
Reason: Fungal contamination of affected lot with Parengyodontium album.
Root cause: Under Investigation by firm
Recalling firm: Hologic, IncType: Preservative, CytologicalDistribution: US Nationwide distribution.Recall #Z-1093-2026 Open, ClassifiedPosted Jan 15, 2026·Initiated Dec 15, 2025
Plum Duo Infusion System, List Number 40002-04-01
Reason: ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound. If the primary speaker in your Plum Duo Infusion Pump fails, the pump may not produce audible alarms, alerts, or provide audible feedback for touchscreen inputs.
Root cause: Nonconforming Material/Component
Recalling firm: ICU Medical, Inc.Type: Pump, InfusionDistribution: Worldwide - US Nationwide distribution.Recall #Z-1094-2026
Open, ClassifiedPosted Jan 15, 2026·Initiated Dec 11, 2025
The product is used for the evaluation of the intrinsic coagulation pathway, APTT substitution test and the monitoring of
heparin therapy.
Reason: Potential for microbial contamination.
Root cause: Under Investigation by firm
Recalling firm: Instrumentation LaboratoryType: Activated Partial ThromboplastinDistribution: Worldwide - US Nationwide distribution in the states of CA, FL, IL, MN, MS, NE, OH, TX, WI and the countries of Belgium, Netherlands, Luxembourg, Switzerland, China, Hong Kong, Israel, Italy, South Korea, Lithuania, Macao, Malaysia, Philippines, Qatar, Romania, Turkey, Kosovo.Recall #Z-1095-2026 Open, ClassifiedPosted Jan 15, 2026·Initiated Dec 15, 2025
da Vinci SP, SP Access Port Kit, Large Incision
Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075 (2.7-7cm,SP1098,Box)
Reason: Access Port System tray may develop cracks potentially resulting in a sterility breach.
Root cause: Packaging change control
Recalling firm: Intuitive Surgical, Inc.Type: System, Surgical, Computer Controlled InstrumentDistribution: Worldwide - US Nationwide distribution including in the states of Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin and the countries of Australia, Austria, Belgium, China, Czech Republic, Denmark, France, Germany, Greece, Hong Kong, Ireland, Italy, Japan, Poland, Romania, Saudi Arabia, South Korea, Spain, Sweden, Switzerland, Taiwan, United Arab Emirates, United Kingdom.Recall #Z-1096-2026
Open, ClassifiedPosted Jan 15, 2026·Initiated Dec 4, 2025
Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090
AB9G12100090
AB9G14080090
AB9G12080090
AB9U12060090
AB9U14100090
AB9U14080090
AB9U12080090
AB9U14060090
AB9G14100090
AB9G12060090
Reason: Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force. Issue may result in stent migration.
Root cause: Under Investigation by firm
Recalling firm: Medtronic IncType: Stent, Iliac VeinDistribution: Worldwide - US Nationwide and the countries of Argentina, Australia, Austria, Belgium, Chile, Colombia, Costa Rica, Denmark, Dominican Republic, Finland, Germany, Jordan,
Lebanon, Malaysia, Netherlands, New Zealand, Peru, Poland, Russia, Singapore, Spain,
Switzerland, Taiwan, Thailand, United Arab Emirates, United Kingdom, Uzbekistan, Vietnam.Recall #Z-1098-2026 Open, ClassifiedPosted Jan 15, 2026·Initiated Oct 10, 2025
CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016;
CentriMag RVAD HDE KIT, REF: 104318;
CentriMag Pre-connected Pack, REF: CMAEK00;
CentriMag VAD KIT, REF: 201-51006, 201-51007, 201-90001 201-90001T;
Blood Pump with CentriMag Acute Circulatory Support System for ECMO, REF: CMAEK01.
CentriMag Blood Pump is a component to be used with CentriMag Acute Circulatory Support System
Reason: Acute circulatory support system pump may not fit into the motor and reports received of the pump not being securely locked into the motor using the screw-in locking feature. Failure to properly lock the pump into motor my not cause pump not inserted alarm, and could lead to particulate, increased heat, anxiety, inconvenience, delay in hemodynamic/ECMO support, stroke, embolism, death.
Root cause: Process design
Recalling firm: Thoratec LLCType: Blood Pump For Ecmo, Long-Term (> 6 Hours) UseDistribution: Worldwide - US Nationwide distribution including in the states of MN, PA, OK, FL, CA, OR, IL, NY, DE, GA, NJ, NC, WI, OH, AZ, AR, TX, TN, MO, MA, MT, KY, NE, WV, VA, ME, ND, AL, CO, DC, MS, IN, MI, CT, SC, WA, NM, MD, HI, ID, IA, LA, UT, RI, NV and the countries of Algeria, Australia, Austria, Bahrain, CANADA, Cayman Islands, Colombia, Costa Rica, Cyprus, Czech Republic, Denmark, Egypt, Estonia, Finland, France, Germany, Hong Kong, Italy, Jordan, Kuwait, Lithuania, Macedonia, Malaysia, Mexico, Netherlands, Oman, Peru, Poland, Portugal, Qatar, Romania, Russian Fed., Saudi Arabia, Serbia, Singapore, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom.Recall #Z-1099-2026
Open, ClassifiedPosted Jan 15, 2026·Initiated Dec 19, 2025
Pulsator Arterial Blood Sampling Kit, Item Numbers
4044EG-1
4080P-2
4084P-1
4080PE
4080PG
Reason: Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to blood leakage during sampling of arterial blood or leakage during fluid delivery.
Root cause: Under Investigation by firm
Recalling firm: ICU Medical Inc.Type: Tubes, Vials, Systems, Serum Separators, Blood CollectionDistribution: US Nationwide distribution in the states of CA, FL, IL, IN, MA, MI, MN, MO, NE, NJ, NY, OH,
OK, TX, WA.Recall #Z-1100-2026
Open, ClassifiedPosted Jan 15, 2026·Initiated Dec 19, 2025
Portex Spinal Tray, Item No. A3729-24
A3595
Reason: Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to blood leakage during sampling of arterial blood or leakage during fluid delivery.
Root cause: Under Investigation by firm
Recalling firm: ICU Medical Inc.Type: Anesthesia Conduction KitDistribution: US Nationwide distribution in the states of CA, FL, IL, IN, MA, MI, MN, MO, NE, NJ, NY, OH,
OK, TX, WA.Recall #Z-1101-2026
Open, ClassifiedPosted Jan 14, 2026·Initiated Nov 24, 2025
FreeStyle Libre 3 Sensor REF 72081-01
UDI-DI code: 00357599818005
The FreeStyle Libre 3 sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Reason: Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Root cause: Process control
Recalling firm: Abbott Diabetes Care, Inc.Type: Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery SystemsDistribution: U.S.: AK, AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NV, NY, OH, OK, PA, SC, SD, TX, UT, VA, WI, WV, and WY.
O.U.S.: Andorra, Austria, Belgium, Canada, Denmark, Finland, France, Germany, Italy, Luxembourg, Netherlands, New Zealand, Norway, Qatar, San Marino, Spain, Sweden, Switzerland, and United Kingdom.Recall #Z-1020-2026 Open, ClassifiedPosted Jan 14, 2026·Initiated Nov 24, 2025
FreeStyle Libre 3 Plus Sensor REF 78768-01
UDI-DI code: 00357599844011
The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Reason: Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Root cause: Process control
Recalling firm: Abbott Diabetes Care, Inc.Type: Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery SystemsDistribution: U.S.: AK, AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NV, NY, OH, OK, PA, SC, SD, TX, UT, VA, WI, WV, and WY.
O.U.S.: Andorra, Austria, Belgium, Canada, Denmark, Finland, France, Germany, Italy, Luxembourg, Netherlands, New Zealand, Norway, Qatar, San Marino, Spain, Sweden, Switzerland, and United Kingdom.Recall #Z-1021-2026 Open, ClassifiedPosted Jan 14, 2026·Initiated Nov 24, 2025
FreeStyle Libre 3 Plus Sensor REF 78769-01
UDI-DI code: 00357599843014
The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Reason: Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Root cause: Process control
Recalling firm: Abbott Diabetes Care, Inc.Type: Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery SystemsDistribution: U.S.: AK, AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NV, NY, OH, OK, PA, SC, SD, TX, UT, VA, WI, WV, and WY.
O.U.S.: Andorra, Austria, Belgium, Canada, Denmark, Finland, France, Germany, Italy, Luxembourg, Netherlands, New Zealand, Norway, Qatar, San Marino, Spain, Sweden, Switzerland, and United Kingdom.Recall #Z-1022-2026 Open, ClassifiedPosted Jan 14, 2026·Initiated Nov 24, 2025
FreeStyle Libre 3 Plus Sensor REF 72080-01
UDI-DI code: 00357599819002
The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Reason: Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Root cause: Process control
Recalling firm: Abbott Diabetes Care, Inc.Type: Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery SystemsDistribution: U.S.: AK, AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NV, NY, OH, OK, PA, SC, SD, TX, UT, VA, WI, WV, and WY.
O.U.S.: Andorra, Austria, Belgium, Canada, Denmark, Finland, France, Germany, Italy, Luxembourg, Netherlands, New Zealand, Norway, Qatar, San Marino, Spain, Sweden, Switzerland, and United Kingdom.Recall #Z-1023-2026 Open, ClassifiedPosted Jan 14, 2026·Initiated Dec 8, 2025
Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models:
1. Azurion 3 M12. Model Number: 722229.
2. Azurion 3 M15. Model Number: 722230.
3. Azurion 5 M12. Model Number: 722231.
4. Azurion 5 M20. Model Number: 722232.
5. Azurion 7 B12. Model Number: 722235.
6. Azurion 7 B20. Model Number: 722236.
7. Azurion 7 M12. Model Number: 722233.
8. Azurion 7 M20. Model Number: 722234.
Reason: Nine (9) identified software issues which may result in the following: loss of X-ray after Pedal Tap, loss of X-ray after Phase Fault, missing live X-ray on the FlexVision monitor, system continues to restart, AMD triple drive, C-Partition of Suite PC running out of free space, system remains in continuous restart mode after start-up, misalignment of Marker Tool Overlay, longitudinal position error.
Root cause: Software design
Recalling firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Type: Interventional Fluoroscopic X-Ray SystemDistribution: Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Argentina, Australia, Austria, Bangladesh, Belgium, Brazil, Brunei Darussal, Bulgaria, Cambodia, Canada, Chile, Colombia, Cote de'Ivore, Croatia, Czech Republic, Denmark, Dominican Rep, Ecuador, Egypt, El Salvador, Estonia, Finland, France, Germany, Greece, Honduras, Hong Kong, India, Indonesia, Iraq, Israel, Italy, Japan, Kazakhstan, Kosovo, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Mauritius, Morocco, Nepal, Netherlands, New Zealand, Nicaragua, Norway, Oman, Palestine, Philippines, Poland, Portugal, R¿union, Romania, Saudi Arabia, Serbia, Singapore, South Africa, South Korea, Spain, Sri Lanka, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkiye, Ukraine, United Kingdom, Utd.Arab.Emir., Uzbekistan, Vietnam, Yemen.Recall #Z-1079-2026
Open, ClassifiedPosted Jan 14, 2026·Initiated Dec 9, 2025
Brand Name: PALACOS
Product Name: PALACOS R pro 40; PALACOS R pro 80
Model/Catalog Number: 5081286; 5081287
Software Version: N/A
Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).
Component: N/A
Reason: increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.
Root cause: Under Investigation by firm
Recalling firm: Heraeus Medical GmbH (Dental Division)Type: Bone CementDistribution: International distribution in the countries of Aland Islands, Australia, Belgium, Denmark, Finland, Germany, Ireland, Italy, Liechtenstein, Netherlands, New Zealand, Norway, Portugal, Spain, Sweden, Switzerland, United Kingdom.Recall #Z-1080-2026
Open, ClassifiedPosted Jan 14, 2026·Initiated Dec 9, 2025
Brand Name: PALACOS
Product Name: PALACOS R+G pro 40; PALACOS R+G pro 80
Model/Catalog Number: 5081288; 5081289
Software Version: N/A
Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).
Component: N/A
Reason: increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.
Root cause: Under Investigation by firm
Recalling firm: Heraeus Medical GmbH (Dental Division)Type: Bone CementDistribution: International distribution in the countries of Aland Islands, Australia, Belgium, Denmark, Finland, Germany, Ireland, Italy, Liechtenstein, Netherlands, New Zealand, Norway, Portugal, Spain, Sweden, Switzerland, United Kingdom.Recall #Z-1081-2026
Open, ClassifiedPosted Jan 14, 2026·Initiated Dec 9, 2025
Brand Name: PALACOS
Product Name: PALACOS MV+G pro 40; PALACOS MV+G pro 80
Model/Catalog Number: 5081290; 5081291
Software Version: N/A
Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).
Component: N/A
Reason: increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.
Root cause: Under Investigation by firm
Recalling firm: Heraeus Medical GmbH (Dental Division)Type: Bone CementDistribution: International distribution in the countries of Aland Islands, Australia, Belgium, Denmark, Finland, Germany, Ireland, Italy, Liechtenstein, Netherlands, New Zealand, Norway, Portugal, Spain, Sweden, Switzerland, United Kingdom.Recall #Z-1082-2026
Open, ClassifiedPosted Jan 14, 2026·Initiated Dec 9, 2025
Brand Name: PALACOS
Product Name: PALACOS MV pro 40; PALACOS MV pro 80
Model/Catalog Number: 5150633; 5150635
Software Version: N/A
Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).
Component: N/A
Reason: increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.
Root cause: Under Investigation by firm
Recalling firm: Heraeus Medical GmbH (Dental Division)Type: Bone CementDistribution: International distribution in the countries of Aland Islands, Australia, Belgium, Denmark, Finland, Germany, Ireland, Italy, Liechtenstein, Netherlands, New Zealand, Norway, Portugal, Spain, Sweden, Switzerland, United Kingdom.Recall #Z-1083-2026
Open, ClassifiedPosted Jan 14, 2026·Initiated Dec 15, 2025
Asserachrom HPIA.
Model/Catalog Number: 00615.
The Asserachrom HPIA kit is intended for the qualitative detection in plasma or serum of the anti-heparin-platelet factor 4 (PF4) antibodies generated during the type II heparin-induced thrombocytopenia (HIT type II) by ELISA.
Reason: Potential for defect for Asserachrom HPIA lot 271288, which can affect every well in the impacted strip and produce negative results.
Root cause: Under Investigation by firm
Recalling firm: Diagnostica Stago, Inc.Type: Platelet Factor 4 RadioimmunoassayDistribution: Worldwide - US Nationwide distribution in the states of AL, CA, FL, GA, HI, IA, MA, MI, NJ, NV, NY, OH, TN, WI and the countries of Belgium, Canada, Denmark, Algeria, Spain, Finland, France, Great Britain, Italy, Lebanon, Saudi Arabia, Uganda.Recall #Z-1084-2026
Open, ClassifiedPosted Jan 14, 2026·Initiated Dec 16, 2025
Medline medical procedure convenience kits labeled as:
1) THORACIC ROBOTICS, REF DYNJ908777B;
2) CARDIAC ROBOTIC WHC KIT-LF, REF DYNJ911359
Reason: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.
Root cause: Under Investigation by firm
Recalling firm: Medline Industries, LPType: Cardiovascular Procedure KitDistribution: US Nationwide distribution.Recall #Z-1085-2026
Open, ClassifiedPosted Jan 14, 2026·Initiated Dec 16, 2025
Medline medical procedure convenience kits labeled as:
1) LAPAROSCOPY CDS-LF, REF CDS860235L;
2) GENERAL LAPAROSCOPIC, REF CDS930223M;
3) LAP CHOLE CDS, REF CDS983678K;
4) LAPAROSCOPY PELV CDS, REF CDS983679K;
5) LAP CHOLE CDS-LF, REF CDS983752M;
6) LAP CHOLE CDS-LF, REF CDS984016B;
7) LAP CHOLE KIT, REF CDS984020P;
8) LAP CHOLE-LF, REF CDS984175J;
9) LAP COLON CDS, REF CDS984849N;
10) GENERAL LAPAROSCOPY CDS, REF CDS985328M;
11) LAP CHOLE, REF DYNJQ9044O;
12) GENERAL LAPAROSCOPY V, REF DYNJS2032F;
13) LAP CHOLE PACK, REF DYNJ26209R;
14) LAP CHOLE PACK, REF DYNJ26209S;
15) GENERAL LAPAROSCOPY PACK, REF DYNJ37459D;
16) DR. BROWN LAP CHOLE PLUS SETUP, REF DYNJ42578G;
17) LAPAROSCOPY GENERAL PACK, REF DYNJ45083G;
18) LAP CHOLE PACK, REF DYNJ51785D;
19) LAPAROSCOPY PACK, REF DYNJ61652A;
20) ENDOSCOPY, REF DYNJ62133A;
21) LAP CHOLE PACK, REF DYNJ66285A;
22) LAPAROSCOPY PACK, REF DYNJ66289B;
23) LAPAROSCOPIC CHOLECYSTECTO, REF DYNJ67296D;
24) LAPAROSCOPY PACK, REF DYNJ68187A;
25) LAP OB PACK, REF DYNJ68741A;
26) LAP CHOLE PACK-LF, REF DYNJ81408A;
27) LAP CHOLE PACK-LF, REF DYNJ81408B;
28) LAP CHOLE PACK, REF DYNJ85318;
29) GENERAL LAPAROSCOPY PACK, REF DYNJ89677;
30) LEX GENERAL LAPAROSCOPY, REF DYNJ900969J;
31) LAP CHOLE, REF DYNJ901126G;
32) BARIATRIC KIT, REF DYNJ901145I;
33) GENERAL LAPAROSCOPY SOMC-LF, REF DYNJ901164M;
34) LAP GASTRIC SLEEVE, REF DYNJ901504L;
35) GENERAL LAP GASTRIC, REF DYNJ901827X;
36) GENERAL LAPAROSCOPY, REF DYNJ901847N;
37) LOU LAP SIGMOID COLON, REF DYNJ901848L;
38) LAP CHOLE, REF DYNJ901870J;
39) LEX BARIATRIC, REF DYNJ902033L;
40) BARIATRIC, REF DYNJ902515K;
41) LAP CHOLE CDS, REF DYNJ902565K;
42) LAP CHOLE, REF DYNJ902995I;
43) LAP CHOLE, REF DYNJ903163L;
44) LAP APPY, REF DYNJ903164L;
45) GENERAL SURGERY LAPAROSCOPY, REF DYNJ903733C;
46) LAP CHOLE, REF DYNJ904693D;
47) BARIATRIC, REF DYNJ904891N;
48) LAPAROSCOPY, REF DYNJ905071F;
49) KIT GENERAL LAPAROSCOPY MHS, REF DYNJ905390F;
50) KIT GENERAL LAPAROSCOPY MHS, REF DYNJ905390G;
51) KIT GENERAL LAPAROSCOPY WEILER, REF DYNJ905407D;
52) KIT GENERAL LAP WAKEFIELD, REF DYNJ905413A;
53) KIT GENERAL LAP WAKEFIELD, REF DYNJ905413B;
54) LAP BARIATRIC, REF DYNJ905733K;
55) KIT LAPAROSCOPIC GASTRIC B, REF DYNJ905856A;
56) LAP CHOLE, REF DYNJ906277D;
57) LAP CHOLE RFD, REF DYNJ906302D;
58) KIT LAP COLON RFD, REF DYNJ906315D;
59) GASTRIC SLEEVE, REF DYNJ906355D;
60) PROSTATECTOMY LAP ROBOTIC, REF DYNJ906805C;
61) LAP ROBOTIC SURG ONCOLOGY, REF DYNJ906824C;
62) GEN BARIATRIC, REF DYNJ907639D;
63) LAP CHOLE, REF DYNJ908415B;
64) LAP CHOLE, REF DYNJ908415C;
65) LAPAROSCOPIC, REF DYNJ908569B;
66) ROBOTIC GASTRIC LAP SLEEVE-LF, REF DYNJ909119G;
67) LAPAROSCOPIC GASTRIC ADD ON, REF DYNJ909628A;
68) BARIATRIC CENTRASTATE, REF DYNJ909817A;
69) LAP GENERAL THEDA, REF DYNJ910050;
70) LAPAROSCOPIC CHOLE PACK, REF DYNJ910139A;
71) ROBOTIC THORACIC, REF DYNJ910386;
72) BARIATRIC, REF DYNJ911017.