Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,439 recalls have been distributed to Nebraska in the last 12 months.
Showing 30001–30020 of 49,150 recalls
Recalled Item: Delta Recalled by Draegar Medical Systems, Inc. Due to It was reported that...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta XL Recalled by Draegar Medical Systems, Inc. Due to It was reported...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kappa Recalled by Draegar Medical Systems, Inc. Due to It was reported that...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Patient Care Kits Product Usage: A Patient Care Kit Recalled by Alcon...
The Issue: Alcon is initiating a Voluntary Medical Device Removal because the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Craftmatic Model 1 Base for Dual Bed Configurations Recalled by Craftmatic...
The Issue: A potential for dual-configured beds to separate or slip away from one another.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legacy Base for Dual Bed Configurations Recalled by Craftmatic Industries,...
The Issue: A potential for dual-configured beds to separate or slip away from one another.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex Bio-SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex Bio Composite SwiveLock SP Vented Recalled by Arthrex, Inc. Due to...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Recalled...
The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Recalled...
The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Agar (TSA w/ 5% Sheep Blood) Plate Recalled by Remel Inc Due to...
The Issue: Confirmed complaint of surface contamination of Listeria monocytogenes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Medical Radrex - i Digital Radiography X-ray system Radrex-i...
The Issue: It was discovered during a procedure that when the operator made an exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex Recalled by Sysmex America Inc Due to Reported customer complaints of...
The Issue: Reported customer complaints of automated hematology analyzers catching fire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1 mL Medallion¿ Syringe. Catalog Numbers: 701989001 Recalled by Merit...
The Issue: Merit Medical Systems announces a voluntary field action for the 1mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.