Medical Device Recalls
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1 to 3 of 3 Results
PMA Number: P820075 |
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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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Lamicel 20PK 3MM INTL Cervical dilator | 2 | 12/23/2019 | Medtronic Xomed, Inc. |
Lamicel 10PK 10MM INTL | 2 | 12/23/2019 | Medtronic Xomed, Inc. |
Lamicel 20PK 5MM INTL | 2 | 12/23/2019 | Medtronic Xomed, Inc. |
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