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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0179-2020 - Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap. 2 10/23/2019 FEI # 1220799
Andover Healthcare Inc.
Z-0180-2020 - Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap 2 10/23/2019 FEI # 1220799
Andover Healthcare Inc.
Z-0184-2020 - Sterile Co-Flex Med 4" - Product Usage: Single Use secondary wound dressing or compression wrap 2 10/23/2019 FEI # 1220799
Andover Healthcare Inc.
Z-0182-2020 - Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap 2 10/23/2019 FEI # 1220799
Andover Healthcare Inc.
Z-0183-2020 - Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound dressing or compression wrap 2 10/23/2019 FEI # 1220799
Andover Healthcare Inc.
Z-0181-2020 - Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound dressing or compression wrap 2 10/23/2019 FEI # 1220799
Andover Healthcare Inc.
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