Medical Device Recalls
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31 to 37 of 37 Results
Product: kne |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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|---|---|---|---|
| KNEE ARTHROSCOPY PK 4/CS Used by medical staff to perform surgical procedures and patient care p... | 2 | 09/03/2015 |
FEI # 2648727 Customed, Inc |
| Knee Stem Extensions & Impactor Sleeve: STEM IMPLANT 20MMDX145MM STEM IMPLANT 22MMDX145MM STEM IM... | 2 | 08/26/2014 |
FEI # 1000220733 Zimmer, Inc. |
| Knee Instrument Fixation Screws: 48MM HEADED SCREW 48MM HEADLESS SCREW MIS HEADED SCREW, 48MM M... | 2 | 08/26/2014 |
FEI # 1000220733 Zimmer, Inc. |
| Knee Components: ROTULE "913" D=32 , Part Number PGA00030, Lot Number X02383380 INSERT TIBIAL "913... | 2 | 10/31/2012 |
FEI # 1043534 Wright Medical Technology Inc |
| Knee walker, one unit per box. Manufacturer Kenstone Metal (Kunshan) Co., LTD. The intended use is t... | 2 | 06/05/2012 |
FEI # 3002889431 Invacare Corporation |
| KNEE ARTHROSCOPY PACK | 2 | 04/22/2003 |
FEI # 1000125955 Windstone Medical, Inc. |
| KNEE PACK | 2 | 04/22/2003 |
FEI # 1000125955 Windstone Medical, Inc. |
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