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All product recalls associated with Zimmer Inc..
Total Recalls
353
Past Year
7
Class I (Serious)
0
Most Recent
Dec 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The guides may come apart during use, some guides may experience surface cracking, guide handles and modules may not target the femoral nail holes accurately and the instruments may not be able to be assemble together due to a change in the threading method used.
The seal on the sterile barrier pouch may be inadequate, resulting in lack of assurance of sterility.
The seal on the sterile barrier pouch may be inadequate, resulting in lack of assurance of sterility.
The seal on the sterile barrier pouch may be inadequate, resulting in lack of assurance of sterility.
Reamers labeled as having a standard diameter may actually be the dimensions of an Asia reamer, and vice versa.
The corner tab of the inner compartment lid was not folded under before the outer lid was sealed, resulting in lack of assurance of sterility.
The corner tab of the inner compartment lid was not folded under before the outer lid was sealed, resulting in lack of assurance of sterility.
The spacer cutter may jam during surgery, preventing use of the instrument and causing surgical delay.
The threads on the screw are incomplete/non-functional.
The package contains pins with an incorrect diameter.
Drill tip is out of specifications, reducing the efficiency of drilling action, requiring more force and potentially heating the bone surface during operation.
The tyvek lid, which is intended to assure sterility until the device is transported to the operating room, may be missing from the inner tray.
The broach handle may fracture at the threaded tip during use, which would result in surgical intervention to retrieve the broach or the trial as the threaded tip fragment prevents attachment of another handle to retrieve the device.
The implant surface may not have been polished adequately, which could result in increased wear and polyethylene debris generation.
The package is labeled as containing 330 mm length nails, but actually contains 300 mm length nails.
The tibial spacer will not affix to the distal surface of the baseplate, as intended.
The surface finish inside of the broach is not to specification and the instrument may corrode if cleaned and sterilized according to instructions.
Smaller diameter screws than required were included in the package.
The surgical technique is inadequate for extra-small sized implants, resulting in the possibility of the provisional becoming stuck in the bone.
The package contains 11 mm screws instead of the specified 6 mm screws.