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Arrowhead DE Recalls

1 recall on record · August 26, 2026 to August 26, 2026 · Medical Devices

August 26, 2026Medical DevicesFDA

Arrowhead DE LLC recalls Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525, 21-253528, 21-253530, 21-253533, 21-253535, 21-253540,

Hazard: Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection.

Arrowhead DE Recalls | RecallWatchUSA