Orthofix recalls 8mm drill bits with potential lower cutting performance due to design issues. Affected items have specific catalog numbers and lot codes. Consumers should check their product details.
As a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result in lower cutting performance.
Orthofix is recalling 8mm drill bits that may have lower cutting performance because of a design issue. This could affect the drill bits' effectiveness in medical procedures.
The drill bits have a geometrical detail that doesn't match the intended design, which could lead to reduced cutting performance. This might impact the precision needed in medical procedures.
Medical professionals using these drill bits for surgical procedures are most likely affected. The recall targets specific batches sold through Orthofix.
Check for the catalog number ref 1-1100101 and lot codes B120: 289813, 289813, 300237, 300238, 273342. These drill bits are used in medical settings and are non-sterile.
Look for the catalog number ref 1-1100101 and lot codes B1200713, 289813, 289813, 300237, 300238, 273342 on the drill bit packaging.
The drill bits have a geometrical detail that doesn't match the intended design, which could result in lower cutting performance.
Check for the catalog number ref 1-1100101 and lot codes B1200713, 289813, 289813, 300237, 300238, 273342 on the packaging.
The recall does not require stopping use; the issue is about lower cutting performance, not safety risks.
We’ve drafted a message you can send Orthofix to request your refund or repair — edit it as you like.
Subject: Recall Z-0380-2020 — Orthofix Orthofix Hello, I own a Orthofix that is covered by recall Z-0380-2020 from Orthofix. 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.
