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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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FDA Recall
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Z-0595-2026 - FlexLab (FLX); Version: FLX-217-10; 2 11/26/2025 FEI # 3010825766
Inpeco S.A.
Z-0596-2026 - FlexLab (FLX); Version: FLX-217-40; 2 11/26/2025 FEI # 3010825766
Inpeco S.A.
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