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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-3064-2026
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HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON E... 2 08/31/2026 FEI # 3012236936
Johnson & Johnson Surgical Vision, Inc.
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