Orthofix recalls specific drill bits due to lower cutting performance from design issues. Affected items have a catalog number and UDI. 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 certain drill bits that may not cut as intended due to a design flaw. This could lead to less effective use of the drill bits in medical procedures.
The drill bits have a geometrical detail that doesn't match the intended design, which can cause lower cutting performance. This means the bits might not function properly during medical procedures.
Medical professionals using these drill bits for surgical procedures are most likely affected. Patients receiving these drill bits during surgery may be at risk.
Check for the catalog number ref 1-1100701 and UDI (01)18033509856099 on the drill bits. The lot numbers B1199835, 289815, 289815, and 273344 are also associated with this recall.
Look for the catalog number ref 1-1100701 and UDI (01)18033509856099 on the drill bits.
The drill bits have a geometrical detail that does not correspond to the intended design, which could result in lower cutting performance.
Check for the catalog number ref 1-1100701 and UDI (01)18033509856099 on the drill bits. The lot numbers B1199835, 289815, 289815, and 273344 are also associated with this recall.
The recall record does not specify a remedy, so there is no action required beyond checking if your drill bits are affected.
We’ve drafted a message you can send Orthofix to request your refund or repair — edit it as you like.
Subject: Recall Z-0383-2020 — Orthofix Orthofix Hello, I own a Orthofix that is covered by recall Z-0383-2020 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.
