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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 instrument is prone to fracture during use.
Sterility compromised. Lack of assurance of sterility, as the packages may not have been sealed on the manufacturer's end.
Sterility compromised. Lack of assurance of sterility, as the packages may not have been sealed on the manufacturer's end.
The screw locking cap may fracture when the surgeon rotates it into the locked position.
Leakage: The kits may disassemble at the fluid collection port, which would present a risk of exposure to blood borne pathogens to health care providers should it occur during use.
The sterility of the device may be compromised due to the possible presence of slits or pinholes in the packaging.
The sterility of the device may be compromised due to the possible presence of slits or pinholes in the packaging.
The sterility of the device may be compromised due to the possible presence of slits or pinholes in the packaging.
Parts missing and incomplete etch: The units may not contain the locking ring or the etched alignment marks on the rim.
Mislabeled as to size; 54mm package contains 46 mm device and vice versa.
Inadequate weld on tracker, knob oversized and poor thread design on attachment screw results in seizing. The instrument may break during use, resulting in surgical delay and an increased risk of infection.
Clip Detachment: The retainer c-clip can detach from the instrument during use and may fall into the surgical wound
The package actually contains a knee patellar implant.
The reamer may lock up on the threads of the reamer body rather than spin freely as intended by design.
The instrument may fracture at the threaded end during intramedullary trialing and leave the distal pilot trial in the humeral canal.
The polyethylene tibial articular surface may not lock into some of the tibial plates.
The device was cut to an incorrect angle, which may result in an incorrect bone cut.
Zimmer Spine, Inc. is conducting a RECALL of all manufacturing lots of ST360 Distal Thread Reduction Guide Pins due to an issue with the thread timing.
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.