Medical Device Recalls
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1 result found
Recall Number: Z-1811-2026 |
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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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| Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US | 2 | 04/10/2026 |
FEI # 3007420694 ARJOHUNTLEIGH POLSKA Sp. z.o.o. |
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