Medical Device Recalls
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1 result found
Recall Number: Z-1941-2023 |
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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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| Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040 | 1 | 06/29/2023 |
FEI # 3005747797 TELEFLEX LLC |
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