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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 17 of 17 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0213-2023 - CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD3-5ST 2 11/11/2022 Carefusion 2200 Inc
Z-0214-2023 - CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD3-6ST 2 11/11/2022 Carefusion 2200 Inc
Z-0215-2023 - CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 7" (17.8CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD3-7ST 2 11/11/2022 Carefusion 2200 Inc
Z-0216-2023 - CareFusion V.Mueller GENESIS SMALL, SHALLOW CONT. 21 X 7" (53.3 X 17.8CM) 3" (7.6CM) DEEP STERRAD COMPATIBLE, REF CD4-3ST 2 11/11/2022 Carefusion 2200 Inc
Z-0217-2023 - CareFusion V.Mueller GENESIS SMALL CONTAINER 21 X 7" (53.3 X 17.8CM) 5-1/2" (14CM) DEEP STERRAD COMPATIBLE, REF CD4-5ST 2 11/11/2022 Carefusion 2200 Inc
Z-0218-2023 - CareFusion V.Mueller GENESIS LARGE, SHALLOW CONT. 28 X 11" (71.1 X 27.9CM) 3" (7.6CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD5-3ST 2 11/11/2022 Carefusion 2200 Inc
Z-0204-2023 - CareFusion V.Mueller GENESIS QTR-LENGTH CONTAINER 12 X 8" (30.3X20.3CM) 4" (10.2CM) DEEP STERRAD COMPATIBLE, REF CD0-4ST 2 11/11/2022 Carefusion 2200 Inc
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