Miach Orthopaedics FDA Recalls

2 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
BEAR Implant. Model Number: 1000.Class IIDec 31, 2025Incorrect expiration date on label that extends beyond the p	Incorrect expiration date on label that extends beyond the product's documented/approved shelf life. With an	Class IIDevices	Dec 31, 2025
BEAR Implant (Bridge-Enhanced ACL Restoration); Model/Catalog: 1000;Class IIFeb 2, 2023The field action was initiated in February of 2023 and was l	The field action was initiated in February of 2023 and was limited to the affected lot from sales force trunk	Class IIDevices	Feb 2, 2023