Medical Device Recalls
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1 result found
Recall Number: Z-1807-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs ... | 2 | 04/17/2026 |
FEI # 3031733296 Uvlizer c/o RAIS INTERNATIONAL LLC |
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