Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K953490 |
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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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Product 62 consists of all product under product code: LPH and same usage: Item no: 620003620 TRI... | 2 | 03/12/2016 | Zimmer Manufacturing B.V. |
TRILOGY ACET SHELL 36MM O TRILOGY ACET SHELL 38MM O TRILOGY ACET SHELL 40MM O TRILOGY ACET SHELL ... | 2 | 02/20/2014 | Zimmer, Inc. |
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