Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K031572 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Xl por st 24.0x220mm, bowed, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee... | 2 | 03/20/2017 | Zimmer Biomet, Inc. |
Xl por st 25.5x220mm, bowed\, bowed, Sterile, Rod, fixation, intramedullary and accessories- Speci... | 2 | 03/20/2017 | Zimmer Biomet, Inc. |
ZMR Over the Junction Instruments for Revision, utilized for the following ZMR devices: Porous Stem,... | 2 | 12/01/2011 | Zimmer Inc. |
ZMR Porous Revision Hip Prosthesis Surgical Technique, utilized for the following ZMR devices: Porou... | 2 | 12/01/2011 | Zimmer Inc. |
Zimmer ZMR Hip System Instructions for Use, utilized for the following ZMR devices: Porous Stem,Nitr... | 2 | 12/01/2011 | Zimmer Inc. |
ZMR Crossover Instrumentation, utilized for the following ZMR devices: Porous Stem,Nitrited Porous R... | 2 | 12/01/2011 | Zimmer Inc. |
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