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U.S. Department of Health and Human Services

Medical Device Recalls
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91 to 100 of 500 Results *
Recall Date to: 07%2F14%2F2014
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FDA Recall
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t:connect mobile app used in conjunction with t:slim X2 insulin pump with Control-IQ technology 1 05/06/2024 Tandem Diabetes Care, Inc.
GE Healthcare Innova IGS 6, Interventional fluoroscopic x-ray systems 2 05/06/2024 GE Medical Systems, SCS
GE Healthcare Interact Discovery RT, Interventional fluoroscopic x-ray systems 2 05/06/2024 GE Medical Systems, SCS
GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems 2 05/06/2024 GE Medical Systems, SCS
GE Healthcare Allia IGS 7, Interventional fluoroscopic x-ray systems 2 05/06/2024 GE Medical Systems, SCS
GE Healthcare Allia IGS 7 OR, Interventional fluoroscopic x-ray systems 2 05/06/2024 GE Medical Systems, SCS
GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems 2 05/06/2024 GE Medical Systems, SCS
GE Healthcare Innova IGS 5, computed tomography x-ray system 2 05/06/2024 GE Medical Systems, SCS
Baxter Spectrum IQ Infusion Pump, Product Code 3570009 2 05/03/2024 Baxter Healthcare Corporation
Clinical Chemistry Calibration Serum (Catalog number Cal2351) that is 20x5ml lyophilized human based... 2 05/03/2024 Randox Laboratories Ltd.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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