In2bones recalls NeoSpan SuperElastic Compression Staple kits with wrong 3mm drill bit (should be 2mm). Affected lots: 9G88C0. Stop using immediately to avoid injury.
The NeoSpan Compression Staple (10x10x10) kits from two lots contain the wrong size drill bit. They contain a 3mm drill bit instead of a 2mm drill bit.
In2bones is recalling NeoSpan SuperElastic Compression Staple kits (Size 10x10x10, Part Number T50 SN010) because some kits contain a 3mm drill bit instead of the required 2mm drill bit. This mismatch could cause injury during use if the wrong bit is used in medical procedures.
Using a 3mm drill bit instead of the required 2mm drill bit could cause the staple to be too large for the tissue, potentially leading to tissue damage or injury during surgery. This mismatch may not cause immediate harm but could result in complications if the staple is used incorrectly.
Medical professionals who use these staples for surgical procedures are most at risk. Patients receiving these staples during surgery could be affected if the wrong drill bit is used.
Check for the lot number 9G88C0 on the NeoSpan SuperElastic Compression Staple kit (Size 10x10x10, Part Number T50 SN010). The kit contains a 3mm drill bit instead of the required 2mm drill bit.
Discontinue use of the recalled NeoSpan SuperElastic Compression Staple kits with lot number 9G88C0 to prevent potential injury.
The recalled NeoSpan SuperElastic Compression Staple kits (Size 10x10x10, Part Number T50 SN010) contain a 3mm drill bit instead of the required 2mm drill bit.
Check for the lot number 9G88C0 on the NeoSpan SuperElastic Compression Staple kit (Size 10x10x10, Part Number T50 SN010).
Stop using the recalled product immediately to prevent potential injury. The manufacturer does not provide a replacement or repair option.
We’ve drafted a message you can send In2bones to request your refund or repair — edit it as you like.
Subject: Recall Z-0670-2019 — In2bones In2bones Hello, I own a In2bones that is covered by recall Z-0670-2019 from In2bones. 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.
