FDA Recalls, Food, Drug & Medical Device Alerts - Page 36 of 46
Latest food, drug, and medical device recalls issued by the U.S. Food and Drug Administration. Class I, II, and III recall classifications, affected products, and consumer guidance.
Showing 1,751–1,800 of 2,262 FDA recalls. Browse by month →
FDA Recalls
FDA Recall of Pelvic Reconstruction System by I.T.S. GmbH
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FDA Recalls
Recall of Philips L12-5 Ultrasound Transducer
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FDA Recalls
Recall of Olympus HALO PKS Cutting Forceps Due to Welding Defect
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FDA Recalls
FDA Recall of MicroScan Neg MIC 56 Due to Contamination
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FDA Recalls high
FDA Recall of Volar Radius Plate by I.T.S. GmbH
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FDA Recalls high
FDA Class I Recall for Erbe USA Inc's Flexible Cryoprobe
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FDA Recalls
FDA Recall for Philips C9-4 Ultrasound Transducer
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FDA Recalls
BiDop 3 Pocket Doppler Recall Issued by FDA
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FDA Recalls
FDA Recall of Olympus PKS Cutting Forceps Due to Welding Defect
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FDA Recalls
Recall of Olympus Everest Bipolar Cutting Forceps
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FDA Recalls
Recall of I.T.S. GmbH Pilon Plates Over MRI Safety Concerns
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FDA Recalls
FDA Recall of Philips X7-2 Ultrasound Transducer
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FDA Recalls
Recall of Philips 3D6-2 Ultrasound Transducer
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FDA Recalls high
Recall of FR.O.H. Calcaneus Repair System Due to MRI Safety Concerns
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FDA Recalls
Recall of Straumann Custom Abutment AS Ti Due to Manufacturing Mix-Up
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FDA Recalls
FDA Recall of Embrace Drill Tower Due to Labeling Error
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FDA Recalls
FDA Announces Recall of I.T.S. DUL and UOL Systems
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FDA Recalls
Recall of Philips OMNI III TEE Ultrasound Transducer Announced
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FDA Recalls
Recall of Philips Mini Multi TEE Ultrasound Transducer
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FDA Recalls
Recall of Humeral Head Plate Devices by I.T.S. GmbH
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FDA Recalls high
Recall of DuraMax Chronic Hemodialysis Catheter Announced
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FDA Recalls high
I.T.S. GmbH Clavicula Plate Recall Over MRI Safety Concerns
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FDA Recalls
Recall of Olympus Everest Bipolar Cutting Forceps Model 3005
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FDA Recalls
Recall of TECNIS Eyhance IOL with Delivery System
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FDA Recalls
I.T.S. GmbH Fibula Plate Recall
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FDA Recalls
Recall of Straumann Custom Abutment Ti Devices
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FDA Recalls
FDA Recall of Olympus Endoscope Air/Water Valve MAJ-1444
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FDA Recalls high
FDA Recall of Handy Solutions Neck & Shoulders Heating Pad
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FDA Recalls high
Recall of BioFlo DuraMax Catheters Due to Design Defect
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FDA Recalls
Recall of Philips L17-5 Ultrasound Transducer for Labeling Clarification
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FDA Recalls
I.T.S. LRS Locking System Recall Due to MRI Safety Concerns
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FDA Recalls
Recall of Olympus Endoscope Reprocessor OER-Elite
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FDA Recalls
FDA Recall of Tandem Insulin Pumps Due to User Guide Errors
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FDA Recalls high
Recall of Merit Medical's 16F Dual Valved Splittable Sheath Introducer
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FDA Recalls
FDA Recall of Olympus PK Cutting Forceps Due to Welding Defect
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FDA Recalls
Recall of Philips OMNI II TEE Ultrasound Transducer
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FDA Recalls
FDA Announces Recall of Philips X3-1 Ultrasound Transducer
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FDA Recalls
FDA Recall of Olympus Endoscope Reprocessor OER-Pro
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FDA Recalls high
Recall of Philips Respironics Trilogy Evo O2 Ventilator for Safety Issue
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FDA Recalls
Recall of Imactis CT-Navigation System by GE Medical Systems
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FDA Recalls
FDA Recall of Philips S4-1 Ultrasound Transducer
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FDA Recalls high
Recall of ProGuide Chronic Dialysis Catheters Due to Design Defect
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FDA Recalls
Recall of Olympus Endoscope Suction Valve MAJ-1443
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FDA Recalls
Recall of I.T.S. Pelvic Reconstruction System Over MRI Safety Concerns
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FDA Recalls high
I.T.S. Straight Plate Recall Due to MRI Safety Issues
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FDA Recalls high
FDA Recall of Flexible Cryoprobe by Erbe USA Inc
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FDA Recalls high
FDA Recall of CentrosFLO Hemodialysis Catheters Due to Design Defect
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FDA Recalls
Recall of Distal Humeral Plates by I.T.S. GmbH
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FDA Recalls
Recall of HLS Hand Locking Plates System by I.T.S. GmbH
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FDA Recalls
Recall of Olympus PKS Cutting Forceps Due to Welding Defect
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