
Stryker · Model Trauma
Full-length X-ray capability. Securely-mounted, lateral C-spine cassette holder. Precisely position slide-out tray for supreme imaging results. 90-degree backrest helps facilitate imaging access.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Pump will not raise the deck, or the deck settles under load.
Root cause: Worn hydraulic pump / seals, an internal valve leak, or low hydraulic fluid.
Symptoms: Brake will not hold, fifth-wheel steer ineffective, castor shimmy.
Root cause: Worn brake linkage, castors, or the fifth-wheel mechanism.
Symptoms: Backrest will not raise / hold, gas strut weak, pneumatic assist failed.
Root cause: Worn gas spring / strut or the release mechanism.
Symptoms: Siderails will not latch or drop, IV pole loose, litter attachments worn.
Root cause: Worn latches, detents, or accessory sockets.
Symptoms: Drive assist will not engage or is weak, drive-fault code.
Root cause: Drive battery, motor / controller, or the throttle.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Hydraulic pump / seal kit | Major service part | $$ | Moderate |
| Castor / brake-linkage set | Periodic replacement | $$ | Moderate |
| Backrest gas spring / strut | Periodic replacement | $$ | Fairly easy |
| Siderail latch / accessory sockets | Major service part | $$ | Fairly easy |
| Drive battery (powered stretchers) | Periodic replacement | $$ | Fairly easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
Synced live from the FDA openFDA API.
A review of packaging revealed the seal integrity of the pouch may be compromised. More specifically, there is a potential that the sterile pouch is not sealed at one end due to a manufacturing error.
It was reported that the secondary locking mechanism, and its corresponding components, disassociated from the Specialty Triathlon Tibial Alignment Handle with Secondary Lock Assembly during surgery. Upon further investigation, it was discovered that the weld, which was intended to hold the secondary locking mechanism together, did not meet the weld size specified on the engineering drawing.
Potential for implant deformation, implant mechanical stability too low, loss of barrier adhesion intra-operatively, implant damage, implant cracking off/breaking intra-operatively.
The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and March 7, 2014 may have been assembled without electrical insulation of the soldering joints
Stryker became aware during laboratory testing that there is a potential that the seal integrity of the outer pouch (sterile barrier) may be compromised for certain lots of the product Teflon Tube, sterile.
Three complaints have been filed where the Hoffman LRF Telescopic Struts have broken during load bearing application by patients having a body weight greater than 250 LBS.
Stryker has become aware that there exists a potential for breach of the sterile barrier of packaging associated with certain lots of T2 Knee Arthrodesis Nails.
There is potential for a breach in sterility in the blister packaging. This can lead to the use of non-sterile product which, if contaminated, could lead to a patient infection.
Instruction for use incorrect: There are no statements or warning on labels or Instructions for Use that 8, 9 and 10 mm diameter MRS Cemented Stems are indicated only for use in the GMRS Proximal Tibial and Distal Femoral Components.
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