Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K073182 |
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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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IUD Insertion Kit | 2 | 10/16/2021 | Stradis Medical, LLC dba Stradis Healthcare |
Tenaculum, Plastic | 2 | 10/16/2021 | Stradis Medical, LLC dba Stradis Healthcare |
IUD Insertion Pack | 2 | 10/16/2021 | Stradis Medical, LLC dba Stradis Healthcare |
Standard IUD Insertion Kit | 2 | 10/16/2021 | Stradis Medical, LLC dba Stradis Healthcare |
Endometrial Biopsy Kit | 2 | 10/16/2021 | Stradis Medical, LLC dba Stradis Healthcare |
Foundation Kit | 2 | 10/16/2021 | Stradis Medical, LLC dba Stradis Healthcare |
GYNDisposables Inc, IUD INSERTION KIT 935K, STERILE, SINGLE USE, Tenaculum 356T, Uterine Sound 906S,... | 2 | 08/15/2011 | GYN Disposables Inc |
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