Open, ClassifiedPosted Sep 25, 2025·Initiated Sep 3, 2025
Allura Xper FD20/10;
Product Code: 722029;
Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Reason: Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit). If this deterioration occurs, motorized movements of the system will become unavailable. Manual movements of the stand (longitudinal, transversal and rotational for ceiling mounted systems and rotational for floor mounted systems) and table longitudinal movements remain available. Imaging (X-ray) functionality remains available.
Root cause: Device 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, Azerbaijan, Bangladesh, Belarus, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Costa Rica, Cuba, Cyprus, Czech Republic, Denmark, Dominican Rep, Ecuador, Egypt, Estonia, Fiji, Finland, France, FrenchPolynesia, Georgia, Germany, Greece, Honduras, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Kosovo, Lao, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Malta, Martinique, Mauritius, Mexico, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Fed., Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syria, Taiwan, Tanzania, Thailand, Tunisia, T¿rkiye, Ukraine, United Kingdom, Uruguay, Utd.Arab.Emir., Uzbekistan, Venezuela, Vietnam, Yemen.Recall #Z-2632-2025
Open, ClassifiedPosted Sep 25, 2025·Initiated Sep 3, 2025
Allura Xper FD20/15;
Product Code: 722058;
Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Reason: Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit). If this deterioration occurs, motorized movements of the system will become unavailable. Manual movements of the stand (longitudinal, transversal and rotational for ceiling mounted systems and rotational for floor mounted systems) and table longitudinal movements remain available. Imaging (X-ray) functionality remains available.
Root cause: Device 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, Azerbaijan, Bangladesh, Belarus, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Costa Rica, Cuba, Cyprus, Czech Republic, Denmark, Dominican Rep, Ecuador, Egypt, Estonia, Fiji, Finland, France, FrenchPolynesia, Georgia, Germany, Greece, Honduras, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Kosovo, Lao, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Malta, Martinique, Mauritius, Mexico, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Fed., Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syria, Taiwan, Tanzania, Thailand, Tunisia, T¿rkiye, Ukraine, United Kingdom, Uruguay, Utd.Arab.Emir., Uzbekistan, Venezuela, Vietnam, Yemen.Recall #Z-2633-2025
Open, ClassifiedPosted Sep 25, 2025·Initiated Sep 3, 2025
Allura Xper FD20/15 OR Table;
Product Code: 722059;
Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Reason: Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit). If this deterioration occurs, motorized movements of the system will become unavailable. Manual movements of the stand (longitudinal, transversal and rotational for ceiling mounted systems and rotational for floor mounted systems) and table longitudinal movements remain available. Imaging (X-ray) functionality remains available.
Root cause: Device 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, Azerbaijan, Bangladesh, Belarus, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Costa Rica, Cuba, Cyprus, Czech Republic, Denmark, Dominican Rep, Ecuador, Egypt, Estonia, Fiji, Finland, France, FrenchPolynesia, Georgia, Germany, Greece, Honduras, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Kosovo, Lao, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Malta, Martinique, Mauritius, Mexico, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Fed., Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syria, Taiwan, Tanzania, Thailand, Tunisia, T¿rkiye, Ukraine, United Kingdom, Uruguay, Utd.Arab.Emir., Uzbekistan, Venezuela, Vietnam, Yemen.Recall #Z-2634-2025
Open, ClassifiedPosted Sep 25, 2025·Initiated Sep 3, 2025
Allura CV20;
Product Code: 722031;
Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Reason: Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit). If this deterioration occurs, motorized movements of the system will become unavailable. Manual movements of the stand (longitudinal, transversal and rotational for ceiling mounted systems and rotational for floor mounted systems) and table longitudinal movements remain available. Imaging (X-ray) functionality remains available.
Root cause: Device 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, Azerbaijan, Bangladesh, Belarus, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Costa Rica, Cuba, Cyprus, Czech Republic, Denmark, Dominican Rep, Ecuador, Egypt, Estonia, Fiji, Finland, France, FrenchPolynesia, Georgia, Germany, Greece, Honduras, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Kosovo, Lao, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Malta, Martinique, Mauritius, Mexico, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Fed., Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syria, Taiwan, Tanzania, Thailand, Tunisia, T¿rkiye, Ukraine, United Kingdom, Uruguay, Utd.Arab.Emir., Uzbekistan, Venezuela, Vietnam, Yemen.Recall #Z-2635-2025
Open, ClassifiedPosted Sep 25, 2025·Initiated Aug 6, 2025
Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000.
The VASOVIEW HEMOPRO 3 Endoscopic Vessel Harvesting (EVH) System (VH-6000, VH-6001, and VH-6010) is a vessel harvesting kit designed for use with a 7 mm endoscope to cut and cauterize vessel branches. The HP3 Harvesting Tool features two curved, insulated jaws with heating elements that operate through heat and pressure rather than radiofrequency energy.
Reason: Reports of out-of-box failures discovered during the limited launch phase. Failure modes included angled deformity at the attachment site of the Harvesting Tool Jaws and the distal end of the Harvesting Tool Shaft, jaws not fully closed out of box, and heater wire lifted/flexed away from jaws.
Root cause: Under Investigation by firm
Recalling firm: Maquet Cardiovascular, LLCType: Electrosurgical, Cutting & Coagulation & AccessoriesDistribution: US Nationwide distribution in the states of FL, IL, MD & TX.Recall #Z-2636-2025
Open, ClassifiedPosted Sep 24, 2025·Initiated Jul 15, 2025
Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034
Reason: Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.
Root cause: Component change control
Recalling firm: Stryker CommunicationsType: Light, Surgical, Ceiling MountedDistribution: US Nationwide distribution in the states of TX, IL, NY, UT, OR, AZ, VT, NY, IL, MN.Recall #Z-2620-2025
Open, ClassifiedPosted Sep 24, 2025·Initiated Jul 3, 2025
t:slim X2 Insulin Pump with Interoperable Technology (with Tandem t:slim mobile app)
Reason: an app
defect that occurs when the phone is set to a right-to-left language, which causes app-pump pairing issues and
graphical defects, which can potentially lead to incorrect therapy decisions and subsequent hypoglycemia or
hyperglycemia.
Root cause: Software design
Recalling firm: Tandem Diabetes Care, Inc.Type: Alternate Controller Enabled Insulin Infusion PumpDistribution: International distribution to the country of Israel.Recall #Z-2621-2025
Open, ClassifiedPosted Sep 23, 2025·Initiated Aug 28, 2025
Extractor Pro RX Retrieval Balloon Catheter;
UPN (REF): (1) M00547030 (9-12mm Below), (2) M00547000 (9-12mm Above);
Reason: The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.
Root cause: Process control
Recalling firm: Boston Scientific CorporationType: Stents, Drains And Dilators For The Biliary DuctsDistribution: US Nationwide distribution in the states of CA, CO, GA, ID, IL, IN, MA, ME, MI, MS, NC, OH, OK, PA, SD, TN, TX, VA, WA.Recall #Z-2618-2025 Open, ClassifiedPosted Sep 23, 2025·Initiated Sep 9, 2025
Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080
Reason: The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton are JuggerKnot 1.4mm Short devices.
Root cause: Under Investigation by firm
Recalling firm: Biomet, Inc.Type: Fastener, Fixation, Nondegradable, Soft TissueDistribution: US Nationwide distribution.Recall #Z-2619-2025
Open, ClassifiedPosted Sep 22, 2025·Initiated Jul 28, 2025
Ortoma Inserter Adapter OTD:
Inserter Adapter OTD Straight REF 30-201
Model Number: 2001
UDI-DI code: 07350137521019
Inserter Adapter OTD Pinnacle Straight REF 30-202
Model Number: 1001
UDI-DI code: 07350137520593
Reamer Adapter OTD REF 30-157
Model Number: 1003
UDI-DI code: 07350137520081
Inserter Adapter OTD REF 30-158
Model Number: 1004
UDI-DI code: 07350137520098
The Inserter Adapters are intended to be attached to a Cup Inserter Tool. The Cup Inserter Tool (impactor) is intended to be tracked by and navigated to orient and position the hip implant cup correctly relative to preoperative planned position and orientation.
Reason: Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.
Root cause: Process control
Recalling firm: ORTOMA ABType: Orthopedic Stereotaxic InstrumentDistribution: Worldwide - U.S. Nationwide distribution in the state of FL and the countries of Japan, Sweden.Recall #Z-2615-2025
Open, ClassifiedPosted Sep 19, 2025·Initiated Jul 25, 2025
Medline medical convenience kits labeled as:
1. ADULT INTUBATION TRAY, Kit Number ACC010369B;
2. ADULT ICU INTUBATION TRAY, Kit Number ACC010379A;
3. INTUBATION TRAY, Kit Number ACC010392;
4. INTUBATION KIT, Kit Number ACC010467A;
5. ADULT AIRWAY TRAY, Kit Number ACC010469;
6. TRAY 2 INTUBATION DRAWER, Kit Number ACC010480;
7. TRAY 2 INTUBATION DRAWER, Kit Number ACC010480A;
8. ADULT INTUBATION, Kit Number ACC010540;
9. DIFFICULT AIRWAY TRAY #1, Kit Number ACC010593A;
10. DIFFICULT AIRWAY TRAY #1, Kit Number ACC010593B;
11. INTUBATION TRAY, Kit Number DYNDA1847A;
12. INTUBATION TRAY (ADULT), Kit Number DYNJAA245A.
Reason: Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.
Root cause: Component design/selection
Recalling firm: MEDLINE INDUSTRIES, LP - NorthfieldType: Circuit, Breathing (W Connector, Adaptor, Y Piece)Distribution: US distribution to: AL, CA, DE, OR, TN, TXRecall #Z-2566-2025
Open, ClassifiedPosted Sep 19, 2025·Initiated Jul 25, 2025
Medline medical convenience kits labeled as:
1. NEWBORN RESUSCITATION KIT, Kit Number ACC010381C;
2. DRAWER 5 - POSITION 3, Kit Number ACC010532;
3. DRAWER #4C ADULT, Kit Number ACC010671;
4. DRAWER #2, Kit Number ACC010728.
Reason: Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.
Root cause: Component design/selection
Recalling firm: MEDLINE INDUSTRIES, LP - NorthfieldType: General Surgery TrayDistribution: US distribution to: AL, CA, DE, OR, TN, TXRecall #Z-2567-2025
Open, ClassifiedPosted Sep 19, 2025·Initiated Aug 20, 2025
Automated Impella Controller (AIC) with the below brands and product codes. Used with heart assist pump.
1. Impella Controller, Packaged, US; Product Code: 0042-0000-US.
2. Impella Controller, Packaged, US, Loaner; Product Code: 0042-0000-US-L.
3. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA.
4. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU.
5. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK.
6. Impella Controller, UK, Loaner; Product Code: 0042-0000-UK-L.
Reason: Specific Automated Impella Controllers (AICs) that have a Pump Driver Circuit Assembly do not meet current specifications. This may lead to decreased pump performance or pump stop and trigger an Impella Failure or Impella Stopped Controller Failure alarm.
Root cause: Device Design
Recalling firm: Abiomed, Inc.Type: Temporary Non-Roller Type Left Heart Support Blood PumpDistribution: US distribution to AR, AZ, CA, CO, CT, FL, GA, ID, MA, MI, MO, MS, NJ, NY, OH, PA, TX. International distribution to Canada, Germany, Great Britian, Italy, Netherlands, Norway.Recall #Z-2568-2025 Open, ClassifiedPosted Sep 19, 2025·Initiated Aug 8, 2025
Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8 m), Product Code REF 2C8519; intravascular administration set
Reason: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.
Root cause: Under Investigation by firm
Recalling firm: Baxter Healthcare CorporationType: Set, Administration, IntravascularDistribution: US Nationwide distribution.Recall #Z-2594-2025
Open, ClassifiedPosted Sep 19, 2025·Initiated Aug 13, 2025
Philips CT systems labeled as the following:
1. Brilliance CT 40 Channel, Model Number: 728235.
2. Brilliance CT 64 Channel, Model Number: 728231.
3. Ingenuity Flex, Model Number: 728317
Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Root cause: Process control
Recalling firm: Philips North America LlcType: System, X-Ray, Tomography, ComputedDistribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Czech Republic, Denmark, Egypt, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Latvia, Lebanon, Mauritius, Mexico, Netherlands, Norway, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, T¿rkiye, United Kingdom, Utd.Arab.Emir., Vietnam.Recall #Z-2595-2025 Open, ClassifiedPosted Sep 19, 2025·Initiated Aug 13, 2025
Philips CT systems labeled as the following:
1. Brilliance 16 Power, Model Number: 728240.
2. Brilliance CT 16 Slice, Model Number: 728246.
3. Brilliance CT 6 Slice, Model Number: 728256.
Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Root cause: Process control
Recalling firm: Philips North America LlcType: System, X-Ray, Tomography, ComputedDistribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Czech Republic, Denmark, Egypt, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Latvia, Lebanon, Mauritius, Mexico, Netherlands, Norway, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, T¿rkiye, United Kingdom, Utd.Arab.Emir., Vietnam.Recall #Z-2596-2025 Open, ClassifiedPosted Sep 19, 2025·Initiated Aug 13, 2025
Philips CT systems labeled as the following:
1. Big Bore RT, Model Number: 728242.
2. Brilliance CT Big Bore Oncology, Model Number: 728243.
3. Brilliance CT Big Bore, Model Number: 728244.
Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Root cause: Process control
Recalling firm: Philips North America LlcType: System, X-Ray, Tomography, ComputedDistribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Czech Republic, Denmark, Egypt, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Latvia, Lebanon, Mauritius, Mexico, Netherlands, Norway, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, T¿rkiye, United Kingdom, Utd.Arab.Emir., Vietnam.Recall #Z-2597-2025 Open, ClassifiedPosted Sep 19, 2025·Initiated Aug 13, 2025
Philips CT systems labeled as the following:
1. Brilliance iCT, Model Number: 728306.
Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Root cause: Process control
Recalling firm: Philips North America LlcType: System, X-Ray, Tomography, ComputedDistribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Czech Republic, Denmark, Egypt, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Latvia, Lebanon, Mauritius, Mexico, Netherlands, Norway, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, T¿rkiye, United Kingdom, Utd.Arab.Emir., Vietnam.Recall #Z-2598-2025 Open, ClassifiedPosted Sep 19, 2025·Initiated Aug 13, 2025
Philips CT systems labeled as the following:
1. Brilliance iCT SP, Model Number: 728311.
Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Root cause: Process control
Recalling firm: Philips North America LlcType: System, X-Ray, Tomography, ComputedDistribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Czech Republic, Denmark, Egypt, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Latvia, Lebanon, Mauritius, Mexico, Netherlands, Norway, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, T¿rkiye, United Kingdom, Utd.Arab.Emir., Vietnam.Recall #Z-2599-2025 Open, ClassifiedPosted Sep 19, 2025·Initiated Aug 13, 2025
Philips CT systems labeled as the following:
1. Ingenuity CT 728326, Model Number: 728321.
2. Ingenuity CT 728326, Model Number: 728323.
3. Ingenuity CT, Model Number: 728326.
Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Root cause: Process control
Recalling firm: Philips North America LlcType: System, X-Ray, Tomography, ComputedDistribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Czech Republic, Denmark, Egypt, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Latvia, Lebanon, Mauritius, Mexico, Netherlands, Norway, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, T¿rkiye, United Kingdom, Utd.Arab.Emir., Vietnam.Recall #Z-2600-2025