Zimmer GmbH Recalls Cannulated Drills Due to Potential Material Deviation
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the specifications. The products were distributed to 41 US states.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II recall involving a potential material deviation with no reported injuries or illnesses, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Zimmer GmbH is recalling the Drill, cannulated, 3x90mm, round shaft, Item Number 502015630. An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. All items marked with "Normed" are affected.
The products were distributed to the following US states: AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and WY.
Healthcare providers should stop using the affected devices and contact Zimmer GmbH for further instructions. The source text does not report any illnesses or injuries associated with this recall.
The recalled product
- Product
- Drill, cannulated, 3x90mm, round shaft, Item Number 502015630
- Manufacturer
- Zimmer GmbH
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All items marked with "Normed" are affected
Distribution
Part of a larger recall action
This product is one of 76 recalled by Zimmer GmbH under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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