Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,436 recalls have been distributed to Idaho in the last 12 months.
Showing 19721–19740 of 27,833 recalls
Recalled Item: Norian Drillable Inject 3 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 5 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima 1.5T MR430s MR Scanner Recalled by GE Healthcare, LLC Due to The gas...
The Issue: The gas venting may not occur properly. A site reported a magnet quenching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products AFP Reagent Pack Recalled by ORTHO-CLINICAL...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed that specific lots of VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MSK 1.5T Extreme MR Scanner Recalled by GE Healthcare, LLC Due to The gas...
The Issue: The gas venting may not occur properly. A site reported a magnet quenching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Revolution CT The system is intended for head Recalled by GE Healthcare,...
The Issue: GEHC has become aware of a potential safety issue in the Revolution CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...
The Issue: The device was found to have bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The System 83 Plus Recalled by Custom Ultrasonics, Inc. Due to To warn...
The Issue: To warn customers that Custom Ultrasonics, Inc. System 83 Plus AERs should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ariol is an automated scanning microscope and image analysis system....
The Issue: An issue during the manufacturing process caused systems to have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Theratronics cabinet x-ray systems intended for use in the Recalled by...
The Issue: It was discovered that both the new device and the predicate device failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser...
The Issue: Failure to provide the required instructions specifying a procedure and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Sheridan/HVT Cuffed Recalled by Teleflex Medical Due to The labeling...
The Issue: The labeling of some units indicates that it contains a size 7mm tracheal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker PowerPRO (XT Recalled by Stryker Medical Division of Stryker...
The Issue: Complaints of smoke coming from the foot end of the cot. This reportedly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Recalled...
The Issue: Failure to provide the required instructions specifying a procedure and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herbert Cannulated Bone Screw System Recalled by Zimmer Manufacturing B.V....
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Periarticular plating system Recalled by Zimmer Manufacturing B.V. Due to A...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping Recalled by...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping Recalled by...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis PRECISE (R) RX Nitinol Stent System (Biliary) Recalled by Cordis...
The Issue: Inability to deploy the stent or partial stent deployment.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.