Medical Device Recalls
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1 result found
510(K) Number: K955805 |
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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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| AirLife® MiniSpacer® MDI Dispenser Adapter. Dual-Spray MiniSpacer® Metered Dose Inhaler (MDI) Dispen... | 2 | 07/02/2012 |
FEI # 2026894 Thayer Medical Corporation |
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