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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 28 Results
Related Medical Device Recalls
 
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Z-1706-2018 - BEQ-T 9410 Lurie Chldns Small 1/4, Custom Tubing Kit, Catalog No. 709000430 2 05/08/2018 FEI # 1000222374
Datascope Corporation
Z-1733-2018 - BEQ-TOP 50903 Custom ECC Pack-Pedriatric , Custom Tubing Kit, Catalog No. 709000078 2 05/08/2018 FEI # 1000222374
Datascope Corporation
Z-1708-2018 - Adult ECC Pack BEQ-TOP 22300, Catalog No. 701049504 2 05/08/2018 FEI # 1000222374
Datascope Corporation
Z-1709-2018 - BEQ-TOP 5210 ECC Set - Respiratory, Custom Tubing Kit, Catalog No. 701055604R01 2 05/08/2018 FEI # 1000222374
Datascope Corporation
Z-1710-2018 - BEQ-TOP 33500 3/8" ECC PACK, Catalog No. 701053752 2 05/08/2018 FEI # 1000222374
Datascope Corporation
Z-1711-2018 - BEQ-TOP 40700 HUNTINGTON, Catalog No. 701062899 2 05/08/2018 FEI # 1000222374
Datascope Corporation
Z-1712-2018 - BEQ-TOP 22702 ECC W/HMOD 30000, Catalog No. 701051179 2 05/08/2018 FEI # 1000222374
Datascope Corporation
Z-1713-2018 - BO-TOP 20705 SMALL PATIENT 1/4, Catalog No. 701053486 2 05/08/2018 FEI # 1000222374
Datascope Corporation
Z-1714-2018 - BEQ-TOP 22701, Catalog No. 701050790 2 05/08/2018 FEI # 1000222374
Datascope Corporation
Z-1715-2018 - BEQ-TOP 24202 ADULT ECC, Catalog No. 701054295 2 05/08/2018 FEI # 1000222374
Datascope Corporation
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