Medical Device Recalls
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1 to 10 of 28 Results
Related Medical Device Recalls |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-1707-2018 - Small Patient ECC Pack BEQ-TOP 22301, Catalog No. 701049513 | 2 | 05/08/2018 |
FEI # 1000222374 Datascope Corporation |
| Z-1725-2018 - NICU ECC Pack BEQ-TOP 39202, Custom Tubing Kit, Catalog No. 701067313R01 | 2 | 05/08/2018 |
FEI # 1000222374 Datascope Corporation |
| Z-1727-2018 - ECC Small - Respiratory BEQ-TOP 5210, Custom Tubing Kit, Catalog No. 701055604 | 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-1732-2018 - BO-TOP 20700 SMALL PATIENT 3/8, Custom Tubing Kit, Catalog No. 701050966 | 2 | 05/08/2018 |
FEI # 1000222374 Datascope Corporation |
| Z-1731-2018 - BO-TOP 13901 RAPID RESPONSE, Custom Tubing Kit, Catalog No. 701054874 | 2 | 05/08/2018 |
FEI # 1000222374 Datascope Corporation |
| Z-1718-2018 - BEQ-TOP 8504 1/4X1/4 PACK W/QP, Custom Tubing Kit, Catalog No. 701066949R02 | 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-1733-2018 - BEQ-TOP 50903 Custom ECC Pack-Pedriatric , Custom Tubing Kit, Catalog No. 709000078 | 2 | 05/08/2018 |
FEI # 1000222374 Datascope Corporation |
| Z-1720-2018 - BEQ-TOP 50900 Custom ECC Pack-Neonatal 1/4, Custom Tubing Kit, Catalog No. 709000069R02 | 2 | 05/08/2018 |
FEI # 1000222374 Datascope Corporation |
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