Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K072879 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Biomet INNERVUE DISPOSABLE SCOPE KIT 1.2MM WITH CANNULA SET, PRODUCT NUMBER 922141, STERILE | 2 | 03/07/2011 | Biomet, Inc. |
| Biomet INNERVUE DISPOSABLE SCOPE KIT 1.2MM, PRODUCT NUMBER 922140, STERILE | 2 | 03/07/2011 | Biomet, Inc. |
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