Miach Orthopaedics recalls BEAR Implant Model 1000 due to incorrect expiration date on label, which may extend beyond approved shelf life. Affected units have specific UDI and lot numbers.
Incorrect expiration date on label that extends beyond the product's documented/approved shelf life. With an incorrect expiration date, the UDI will also be incorrect.
Miach Orthopaedics is recalling BEAR Implant Model 1000 because the expiration date on the label is incorrect and extends beyond the product's approved shelf life. This could lead to using an implant that has expired, potentially causing safety issues.
The expiration date on the label is incorrect and extends beyond the product's documented shelf life. This means the implant could be expired, which might lead to safety concerns during medical procedures.
Patients who received the BEAR Implant Model 1000 with the specific UDI and lot number 7011098 are affected. Those using the implant for medical procedures are most at risk.
Check for the UDI number (01)00860002987804(17)260228(10)7011098 and lot number 7011098 on the label. The expiration date listed is 02/28/2026.
Verify the UDI number and lot number on the label to confirm if the product is affected.
The expiration date on the label is incorrect and extends beyond the product's approved shelf life, which could lead to safety concerns.
Look for the UDI number (01)00860002987804(17)260228(10)7011098 and lot number 7011098 on the label.
Check the label details to confirm if the product is affected; no specific action is required beyond verification.
We’ve drafted a message you can send Miach Orthopaedics to request your refund or repair — edit it as you like.
Subject: Recall Z-1220-2026 — Miach Orthopaedics Miach Orthopaedics Hello, I own a Miach Orthopaedics that is covered by recall Z-1220-2026 from Miach Orthopaedics. 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.
