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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.
Lack of assurance of proper metal fatigue strength due to a metal grain structure anomaly.
Lack of assurance of proper metal fatigue strength due to a metal grain structure anomaly.
Components may not lock together as intended.
Lack of assurance of sterility, as the sterile barrier packaging may have been compromised.
Lack of assurance of sterility, as the sterile barrier packaging may have been compromised.
Lack of assurance of sterility, as the sterile barrier packaging may have been compromised.
Lack of assurance of sterility, as the sterile barrier packaging may have been compromised.
During provisional trialing, the instrument may become stuck in the humeral canal and require surgical removal.
The three-point array may break during use, resulting in surgical delay and an increased risk of infection.
Misbranded-The package actually contains an APR hip system, HA porous stem, 12 mm, left.
A c-clip located near the rasp connection end of the instrument may detach during use and fall into the patient.
A c-clip located near the rasp connection end of the instrument may detach during use and fall into the patient.
A c-clip located near the rasp connection end of the instrument may detach during use and fall into the patient.
The devices may fracture, resulting in surgical delay or the need for intervention to remove fragments from the surgical site.
The devices may fracture, resulting in surgical delay or the need for intervention to remove fragments from the surgical site.
The calibrations on the reamers may lead to inaccurate reaming depth when used in accordance with the published surgical technique.
The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement.
May be mislabeled as to dimensions; may be 12/14 taper, 28mm dia., neck length +3.5mm.
The engraved calibration lines are incorrectly specified, which will result in the user obtaining a reading that the chiseling removed material to a depth 10mm deeper than what was actually removed, thus guiding the user to select a blade plate that is longer than will fit.
Risk of adapter disassociation from mating components when assembled improperly or when subjected to high-stress femoral applications.