Medical Device Recalls
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1 result found
Recall Number: Z-3276-2026 |
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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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| Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA | 2 | 09/25/2026 |
FEI # 3008363989 Volcano Corp |
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