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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0107-2018 - Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T) 2 11/18/2017 Medtronic Inc.
Z-0108-2018 - Medtronic MiniMed(TM) Silhouette(TM) (MMT-377, 377T, 378, 378T, 384, 384T, 368, 368T, 381, 381T, 382, 382T, 383, 383T) 2 11/18/2017 Medtronic Inc.
Z-0111-2018 - Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281) 2 11/18/2017 Medtronic Inc.
Z-0110-2018 - Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965, 965T, 975, 975T) 2 11/18/2017 Medtronic Inc.
Z-0109-2018 - Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, 862T, 864, 864T, 866, 866T, 874, 874T, 876, 876T, 884, 886, 886T) 2 11/18/2017 Medtronic Inc.
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