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U.S. Department of Health and Human Services

Medical Device Recalls

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21 to 30 of 168 Results
Class 1 Recall Date from: 01/01/2022 Recall Date to: 12/31/2022
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Product Description
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Philips Respironics V60 Ventilator Part Number 1053617 1 02/25/2022 FEI # 2518422
Respironics California, LLC
Philips Respironics V60 Plus Ventilator Part Number 1138747 1 02/25/2022 FEI # 2518422
Respironics California, LLC
Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02 1 03/02/2022 FEI # 3015423092
CELLTRION USA INC
Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02 1 03/02/2022 FEI # 3015423092
CELLTRION USA INC
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Multi-vessel, Catalog number THP-M. For ... 1 03/07/2022 FEI # 2183870
ev3 Inc.
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Small Vessel, Catalog number THP-S. For... 1 03/07/2022 FEI # 2183870
ev3 Inc.
LuSys 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114(Saliva Test) 1 03/10/2022 FEI # 3004473533
Lusys Laboratories, Inc.
Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114... 1 03/10/2022 FEI # 3004473533
Lusys Laboratories, Inc.
COVID-19 IgG/IGM Antibody Test For Detection of COVID-19 IgG and IgM antibodies Catalog No: I-111 1 03/10/2022 FEI # 3004473533
Lusys Laboratories, Inc.
STANDARD Q COVID-19 Ag Home Test STANDARD Q COVID-19 Ag Home Test is a rapid chromatographic immu... 1 03/16/2022 FEI # 3012133212
SD Biosensor, Inc.
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