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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
510(K) Number: K965016
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Product Description
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Recall
Class
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FDA Recall
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Filter + Catheter Mount, REF 191667-000100, OUS only. Catheter mount for circuit-patient connection ... 1 10/14/2022 TELEFLEX LLC
Iso-Gard Filter S with Expandi-Flex/Elbow: a) REF 19012, OUS only, b) REF 19012T with Tethered Cap,... 1 10/14/2022 TELEFLEX LLC
Iso-Gard Filter S, REF : a) 19211, OUS only; b) 19212; Microbial medical gas filter, single-use. B... 1 10/14/2022 TELEFLEX LLC
Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical ... 1 10/14/2022 TELEFLEX LLC
Iso-Gard Filter S, with Expandi-Flex, REF: a) 19261, OUS only; b) 19272, OUS only; Microbial medic... 1 10/14/2022 TELEFLEX LLC
Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only; b) 19262T, OUS only; c... 1 10/14/2022 TELEFLEX LLC
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