Medical Device Recalls
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1 to 10 of 40 Results
510(K) Number: K042696 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CMEAmerica BodyGuard Wall Charger: Lot number 2019-0364, Mode/Catalogue number 151-143XL, *+B 011511... | 2 | 10/29/2020 |
FEI # 3006967710 CME America LLC |
| CMExpress Microbore Set, REF: A120-161CYF | 1 | 07/15/2020 |
FEI # 3006967710 CME America, LLC |
| BodyGuard Microset With Female Luer, REF: A120-160XPSN | 1 | 07/15/2020 |
FEI # 3006967710 CME America, LLC |
| BodyGuard BodySet, REF: A120-160SAS | 1 | 07/15/2020 |
FEI # 3006967710 CME America, LLC |
| BodyGuard Microset, REF: A120-160XPS | 1 | 07/15/2020 |
FEI # 3006967710 CME America, LLC |
| BodyGuard Microset, REF: A100-163XESV | 1 | 07/15/2020 |
FEI # 3006967710 CME America, LLC |
| BodyGuard Microset, REF: A100-163XES | 1 | 07/15/2020 |
FEI # 3006967710 CME America, LLC |
| BodyGuard Microset, REF: A120-161XPS | 1 | 07/15/2020 |
FEI # 3006967710 CME America, LLC |
| BodyGuard Microset, REF: A120-160XSFK | 1 | 07/15/2020 |
FEI # 3006967710 CME America, LLC |
| BodyGuard Microset, REF: A120-112XSFK | 1 | 07/15/2020 |
FEI # 3006967710 CME America, LLC |
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