Zimmer recalls AO cannulated 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 may have been made from an incorrect material. This could affect how the drills function properly in medical procedures.
The drills might not meet the intended specifications because they were made from a different material than required. This could lead to improper performance during surgical procedures.
Medical professionals using Zimmer AO cannulated drills with "Normed" marking are likely affected. Patients using these drills during surgery may be at slightly higher risk.
Check for the "Normed" marking on the drill. Affected items were sold with the item number ST502015403 and are part of the Zimmer AO cannulated drill series.
Look for the "Normed" marking on the drill to determine if it is affected.
No, only drills marked with "Normed" are affected.
The recall does not specify a remedy, so contact Zimmer directly for guidance.
The recall states a possible material mismatch, but does not mention serious injury risks.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1475-2019 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1475-2019 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.
