Biomet recalls ONPOINT SCOPE PROCEDURE KIT-EU (item 24-3055) due to potential improper sterilization. Affected units have specific lot numbers; consumers should check their product.
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
Biomet is recalling its ONPOINT SCOPE PROCEDURE KIT-EU (item 24-3055) because the product may not be properly sterilized during gamma sterilization. This could lead to contamination risks if used in medical procedures.
The product may not be properly sterilized during gamma sterilization, which could lead to contamination if used in medical procedures. This is a risk during the sterilization process but not a direct hazard in normal use.
Medical professionals using the ONPOINT SCOPE PROCEDURE KIT-EU for surgical procedures are most at risk. The recall affects specific lot numbers of this kit.
Check the item number (24-3055) and lot numbers listed in the recall notice. The affected kits have specific lot numbers starting with 866270A through 947040B.
Look for the lot number on the kit packaging or label to determine if it is affected.
The recall states the product may not be properly sterilized, so it is not safe to use until the recall is addressed.
Check the lot number against the list provided in the recall notice to see if it is affected.
The recall does not specify a replacement or 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-0083-2021 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-0083-2021 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.
