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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
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Z-2251-2024 - BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye) 1 07/11/2024 Synergetics Inc
Z-2254-2024 - BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye) 1 07/11/2024 Synergetics Inc
Z-2253-2024 - BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye) 1 07/11/2024 Synergetics Inc
Z-2252-2024 - BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye) 1 07/11/2024 Synergetics Inc
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