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Astora Recalls
1 recall on record · November 25, 2015 to November 25, 2015 · Medical Devices
November 25, 2015
Medical Devices
FDA
Astora recalls MiniArc Pro Single incision Sling System, Model number / Product Reference 9000261, Lot 936405xxx. Designed to treat fe
Hazard: The lot number on the outer carton label did not match the lot number printed on the tray label or identification labels inside the box. The identification labels inside the box are placed on medical records and other documents associated with the procedure. Use of incorrectly identified labels may prevent direct traceability of the implanted unit in the future.
Astora Recalls | RecallWatchUSA