Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls Recall Date to: 08/04/2015 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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Z-1698-2009 - Zimmer Pulsavac Wound Debridement System high capacity intramedullary brush tip, sterile, Zimmer, Dover, Ohio; Catatog Number: 00515018300. Used in conjunction with the Pulsavac Plus Wound Debridem... | 2 | 07/23/2009 | Zimmer Inc. |
Z-1700-2009 - Zimmer Coonrad/Morrey total elbow cement restrictor with nozzle, 1 - 16 mm, 1 - 25 mm, sterile, Zimmer, Dover, Ohio; Catatog Number: 32810503800. Total joint arthroplasy to control, restrict or imp... | 2 | 07/23/2009 | Zimmer Inc. |
Z-1699-2009 - Zimmer Allen medullary cement plugs, 1 - 20 dia. flange/10 mm dia. core, 1 - 24 mm dia. flange/12 mm dia. core (polyethylene with barium sulfate) with inserter, sterile, Zimmer, Warsaw, Indiana; Catat... | 2 | 07/23/2009 | Zimmer Inc. |
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