Biomet recalls shoulder replacement baseplates that may be shipped with two baseplates and no adapters. This packaging error could lead to improper use during surgery. Affected units include specific item and lot numbers.
Package is intended to contain one (1) baseplate and one (1) taper adapter; however, devices may be packaged with two (2) baseplates and no (0) adapters.
Biomet is recalling shoulder replacement baseplates that might be shipped with two baseplates and no adapters. This packaging error could cause improper surgical use if the wrong components are installed.
The baseplates are intended to be used with one baseplate and one adapter. If two baseplates and no adapters are included, the surgical team may install the wrong components, leading to improper joint function.
Patients who received the recalled shoulder replacement baseplates from Biomet. Surgeons and medical staff who use these components during surgery are most at risk.
Check the product packaging for the item number 01000:00589 and lot number 410420. The UDI code (01) 0 0880304 53246 5 (17) 290825 (10) 410420 may also help identify affected units.
Verify the item number and lot number on the packaging to confirm if it matches the recalled units.
The recall is happening because some shipments contain two baseplates and no adapters, which could lead to improper surgical use.
The official recall notice does not specify a remedy for this issue. Check the packaging for the item number and lot number to confirm if it is affected.
Look for the item number 010000589 and lot number 410420 on the packaging. The UDI code (01) 0 0880304 53246 5 (17) 290825 (10) 410420 may also help identify affected units.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1615-2020 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-1615-2020 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.
