Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K931052 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| a. McKesson DISINFECTANT, GLUTARALDEHYDE 28DAY (4GL/CS) MGM68, Model Number: 68-102800. b. MET... | 2 | 08/26/2022 |
FEI # 3004386693 Mckesson Medical-Surgical Inc. Corporate Office |
| Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution | 2 | 07/05/2019 |
FEI # 2024312 Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical |
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