Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K143299 |
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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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| Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile Manufactured for: Tele... | 2 | 10/07/2016 | Teleflex Medical |
| Teleflex Percuaneous Solutions, Johans Grasper, Ref ML004EE, Rx Only Sterile Manufactured for: Telef... | 2 | 10/07/2016 | Teleflex Medical |
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