Medtronic recalls a single angled drill (REF 6630902) due to a longer drill tip extension than specified, which may cause improper use. Affected units have UDI 00643169363502 and lot number EM17F015.
Medtronic has discovered the product lot in question was noted as having a longer drill tip extension than what is indicated on the print specification.
Medtronic is recalling one angled drill (REF 6630902) that has a longer drill tip extension than specified. This could lead to improper use if the drill is not properly aligned during medical procedures.
The drill tip extension is longer than specified, which could cause misalignment during medical procedures. This might lead to improper use if the drill is not properly aligned with the intended target.
Medical professionals who use this drill for procedures are most at risk. The recall affects only one unit with specific UDI and lot number.
Check for the product reference number 6630902. Affected units have UDI 00643169363502 and lot number EM17F015.
Verify the product reference number and UDI to confirm if your drill is affected.
The recall indicates a potential misalignment risk due to a longer drill tip extension than specified, but it does not state that the drill is dangerous in normal use.
Only one unit with UDI 00643169363502 and lot number EM17F015 is affected.
The recall does not specify a remedy, so check the product details to confirm if it's affected.
We’ve drafted a message you can send Medtr: A short, human brand name for headings (e.g. to request your refund or repair — edit it as you like.
Subject: Recall Z-0566-2018 — Medtr: A short, human brand name for headings (e.g. Medtr: A short, human brand name for headings ( Hello, I own a Medtr: A short, human brand name for headings (e.g. that is covered by recall Z-0566-2018 from Medtr: A short, human brand name for headings (e.g.. 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.
