Recall database

Staple, Fixation, Bone recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–2 of 2 recalls

Class IIOngoingZ-3211-2026

Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established.

F & A FoundationOKSep 23, 2026

Class IIOngoingZ-2355-2026

Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.

In2bones USA, LLCTNJun 17, 2026