Medical Device Recalls
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1 result found
510(K) Number: K963765 |
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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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Stryker, REF: 0250070460, 5.0 mm x 32 cm, Strykeprobe, Outer Sheath Replacement, RX Only, Non-Steril... | 2 | 03/17/2020 | Stryker Corporation |
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