Zimmer recalls AO cannulated 4x120mm drills with "Normed" marking due to possible material mismatch. Affected items may not meet specifications.
An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
Zimmer is recalling certain AO cannulated drills that might be made from an incorrect material. This could affect how the drills function properly.
The drills may not meet the intended specifications because they were possibly made from a different material than required. This could lead to improper function during medical procedures.
Orthopedic surgeons and medical professionals using Zimmer's AO cannulated drills. Those with the specific model marked "Normed" are most at risk.
Check for the model number 502015402 and the "Normed" marking on the drill. These specific items are affected by the recall.
Look for the "Normed" marking on the drill to confirm if it's affected by this recall.
The products were possibly manufactured from a different material than defined in the applicable specifications.
The recall record does not specify a remedy, so check the product marking to see if it's affected.
Drills with the model number 502015402 and the "Normed" marking are affected by this recall.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1435-2019 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1435-2019 from Zimmer. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
