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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K990952
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Ti-Cron Coated Braided Polyester Suture Product Description 88862775-31 TICRON* 4-0 BLU 75CM CV327... 2 02/25/2023 FEI # 1219930
Covidien, LP
Novafil Monofilament Polybutester Suture Product Description: 8886 4002-41 NOVAFIL 3-0 BLU 90CM C... 2 02/25/2023 FEI # 1219930
Covidien, LP
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