Medical Device Recalls
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31 to 33 of 33 Results
510(K) Number: K842648 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Heart Pack, REF numbers: a) 89-9194.07 b) 89-9194.09 c) 89-9194-10 d) 89-9194-11 Custom sur... | 2 | 02/19/2021 | DeRoyal Industries Inc |
Open Heart Pack, REF numbers: a) 89-7483.07 b) 89-7483.08 c) 89-7483.09 d) 89-7483.10 Cus... | 2 | 02/19/2021 | DeRoyal Industries Inc |
Sterile custom surgical procedure packs: (1) 89-10507.02, TOTAL KNEE PACK, Stonewall Jackson Hosp... | 2 | 06/07/2023 | DeRoyal Industries Inc |
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