Biomet recalls Titanium IFS bone fixation devices with specific lot numbers due to potential packaging seal breaches that could compromise sterility.
Specific lots of multiple sterile medical devices may have a breach in the sterile seal. A breach in the packaging seal could lead to loss of sterility of the device.
Biomet is recalling certain Titanium IFS bone fixation devices that may have a breach in the sterile packaging seal. This could lead to loss of sterility, posing a risk of infection during surgery.
A breach in the sterile packaging seal could allow contamination of the device, increasing the risk of infection during surgery. This is a potential sterility issue that could affect the safety of the medical procedure.
Patients scheduled for bone-to-bone surgery using the recalled Titanium IFS devices with lot number 750930 are affected. Surgeons and medical facilities using these specific devices are at risk.
Check for the lot number 750930 on the Titanium IFS bone fixation devices. These devices are used for bone-to-bone fixation and were sold by Biomet.
Look for the lot number 750930 on the device packaging or label.
The specific lot number for this recall is 750930.
Check for the lot number 750930 on the Titanium IFS bone fixation device packaging or label.
The recall does not specify a remedy, so contact Biomet directly for further instructions.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0630-2021 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0630-2021 from Biomet. 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.
