Medtronic Sofamor Danek USA recalls Solera Awl Tip Tap (REF NAV2006K) due to incorrect laser marking. Affected units include specific batch numbers and lot numbers from the SOLERA TAPS Kit.
Incorrect Laser Marking - Solera Awl Tip Tap
Medtronic Sofamor Danek USA is recalling Solera Awl Tip Tap (REF NAV2006K) because of incorrect laser marking. This issue could lead to improper use in spinal surgery procedures.
Incorrect laser marking on the Solera Awl Tip Tap could lead to improper identification or use during spinal surgery. This might cause errors in surgical procedures if the component is not correctly identified.
Surgical professionals using the Solera Awl Tip Tap for spinal procedures are most at risk. Affected units include specific batch numbers and lot numbers from the SOLERA TAPS Kit.
Check for the product code REF NAV2006K on the Solera Awl Tip Tap. Affected units are packaged in the SOLERA TAPS Kit (REF 9735465) with specific batch numbers: 0011743681, 0011734643, 0011713764, 0011722871, 0011705200.
Look for the product code REF NAV2006K on the Solera Awl Tip Tap and check the batch numbers listed in the recall notice.
The hazard is incorrect laser marking on the Solera Awl Tip Tap, which could lead to improper identification during spinal surgery procedures.
Affected batch numbers are 0011743681, 0011734643, 0011713764, 0011722871, and 0011705200.
Check for the product code REF NAV2006K on the Solera Awl Tip Tap and verify the batch numbers listed in the recall notice.
We’ve drafted a message you can send Medtronic Sofamor Dan: a short, human brand name for headings (e.g. to request your refund or repair — edit it as you like.
Subject: Recall Z-2363-2023 — Medtronic Sofamor Dan: a short, human brand name for headings (e.g. Medtronic Sofamor Dan: a short, Hello, I own a Medtronic Sofamor Dan: a short, human brand name for headings (e.g. that is covered by recall Z-2363-2023 from Medtronic Sofamor Dan: 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.
