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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
510(K) Number: K883909
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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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STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567 - Product Usage: The de... 2 05/15/2020 FEI # 2027111
Applied Medical Resources Corp
STEALTH SPRING CLIP 6mm latis (1/4 Force). Non-Sterile, REF/UDI::A1702/(01)10607915110649 - Product ... 2 05/15/2020 FEI # 2027111
Applied Medical Resources Corp
STEALTH SPRING CLIP 6mm latis (3/4 Force). REF/UDI::A1603/(01)00607915110581 - Product Usage: The de... 2 05/15/2020 FEI # 2027111
Applied Medical Resources Corp
STEALTH SPRING CLIP 6mm latis (1/4 Force). REF/UDI::A1602/(01)00607915110574 - Product Usage: The de... 2 05/15/2020 FEI # 2027111
Applied Medical Resources Corp
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