Medical Device Recalls
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151 to 160 of 500 Results
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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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| Ingenia Ambition X, Model No. 782109 | 3 | 01/25/2024 |
FEI # 3006648320 Philips North America |
| Achieva 3.0T, Model No. 781177 | 3 | 01/25/2024 |
FEI # 3006648320 Philips North America |
| Achieva 1.5T Conversion, Model No. 781283 | 3 | 01/25/2024 |
FEI # 3006648320 Philips North America |
| Achieva 1.5T, Model No. 781178, 781196, 781296 | 3 | 01/25/2024 |
FEI # 3006648320 Philips North America |
| Intera 1.5T, Model No. 781195 | 3 | 01/25/2024 |
FEI # 3006648320 Philips North America |
| SEROLOGY ToRCH lgM 2022 POSITIVE CONTROLI Intended for use with in vitro assays for determination of... | 3 | 01/02/2024 |
FEI # 1000361607 Randox Laboratories Ltd. |
| Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111 | 3 | 12/26/2023 |
FEI # 3001451489 Fresenius Medical Care Holdings, Inc. |
| Navik 3D v2, REF NAVIK3D, 3D Mapping System | 3 | 12/14/2023 |
FEI # 3014282601 APN Health LLC |
| Choleodochoscope. Model Numbers: CHF-BP30, CHF-CB30L, CHF-P60. | 3 | 11/17/2023 |
FEI # 3002964398 Aizu Olympus Co., Ltd. |
| KWIK-STIK, ANA (3 Strains) QC Set, REF 5065P; Microbiological testing | 3 | 09/11/2023 |
FEI # 2150138 Microbiologics Inc |
| * The maximium 500 devices meeting your search criteria returned. Please narrow your search. |
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