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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 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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Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/EMEA, REF IAP-0600 (IPN001108), cardiac pump... 1 12/15/2022 FEI # 3013162291
ARROW INTERNATIONAL Inc.
Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-4... 1 12/10/2022 FEI # 3013162291
ARROW INTERNATIONAL Inc.
Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; ... 1 12/10/2022 FEI # 3013162291
ARROW INTERNATIONAL Inc.
Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST 1 12/08/2022 FEI # 1924669
Remel Inc
Thermo SCIENTIFIC, Sensititre HPB1, Gram Negative IVD AST 1 12/08/2022 FEI # 1924669
Remel Inc
Thermo SCIENTIFIC, Sensititre STP7F, Gram Negative IVD AST 1 12/08/2022 FEI # 1924669
Remel Inc
Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST 1 12/08/2022 FEI # 1924669
Remel Inc
Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST 1 12/08/2022 FEI # 1924669
Remel Inc
Thermo SCIENTIFIC, Sensititre CMC5VGNF, Gram Negative IVD AST 1 12/08/2022 FEI # 1924669
Remel Inc
Thermo SCIENTIFIC, Sensititre CMC7AFLF, Gram Negative IVD AST 1 12/08/2022 FEI # 1924669
Remel Inc
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