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U.S. Department of Health and Human Services

Medical Device Recalls

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151 to 160 of 500 Results *
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Product Description
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FDA Recall
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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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