Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K934094 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Stryker, REF: 0250070450, 5.0 mm x 45 cm, Strykeprobe, Outer Sheath Replacement, RX Only, Non-Steril... | 2 | 03/17/2020 | Stryker Corporation |
StrykeFlow 2 System, labeled sterile. Includes the following: a. STRYKER LAPAROSCOPIC SUCTION IR... | 2 | 03/02/2018 | Stryker Corporation |
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