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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-1026-2021
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INJECTOR FORCEMAX UP 2MM CH 23G 3MM, model no. NM-401L-0523 - Product Usage: Used with endoscopes to... 2 02/05/2021 FEI # 3003995201
Aomori Olympus Co., Ltd.
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