Miach Orthopaedics BEAR Implant recall — FDA Z-1220-2026
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.
Overview of recall records associated with Miach Orthopaedics, including dates, categories and classifications where available.
Classification mix: Class II: 1.
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.
This page summarizes recall records in which the official source identifies Miach Orthopaedics as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.