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Extractor

FDA product code HWB · Class 1 · Orthopedic

2,402
Registered devices
3,487
Adverse events
4
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-03-07Innomed, Inc.54 MM finisher blade was inadvertently affixed to the shaft of the CupX handle in lieu of the 54 MM starter blade.
2018-03-19Synthes, Inc.There is a potential for the connection screw of the stem extractor to break.
2010-11-10Encore Medical, LpRevision A and B CLP Extraction Hooks may fracture at the distal end, resulting in surgical delay.
2010-03-02Stryker Howmedica Osteonics Corp.Literature did not include the design change to a smaller cannulation diameter.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.