Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K121566 |
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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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Humidifier bottle and syringe filter kit (6 count of each) for the BT37 Mark II Benchtop Incubator ... | 2 | 09/28/2022 | CooperSurgical, Inc. |
Humidifier bottle and syringe filter kit (6 count of each) for the BT37 Mark I Benchtop Incubator (... | 2 | 09/28/2022 | CooperSurgical, Inc. |
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