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. 2,436 recalls have been distributed to Nebraska in the last 12 months.
Showing 31461–31480 of 49,150 recalls
Recalled Item: Gomco Circumcision Clamps with separate O-Ring Component: The device is...
The Issue: Aesculap has received complaints of excessive bleeding after use of Gomco...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE blanket LED Phototherapy system Recalled by Natus Medical...
The Issue: neoBLUE blanket LED Phototherapy System distributed since release of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices....
The Issue: Breach in sterile barrier compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bupropion Hydrochloride Extended-Release Tablets Recalled by Amerisource...
The Issue: Failed Dissolution Specifications: The firm was notified that there was a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucosal Atomization Device (MAD) Recalled by Teleflex Medical Due to Product...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADomizer Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADdy Recalled by Teleflex Medical Due to Product Defect; These products...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADett Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXI NOZZLE LONG Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXI NOZZLE SHORT Product Usage: These products are used for Recalled by...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADgic Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 Recalled by...
The Issue: CRP samples diluted using VITROS Chemistry Products Specialty Diluent,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Universal Electrosurgical Pad Recalled by 3M Company - Health Care...
The Issue: 3M is recalling Universal Electrosurgical Pads because a report of an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A&W Cream Soda Recalled by Chesterman Co Due to Product is labeled "caffeine...
The Issue: Product is labeled "caffeine free" but testing revealed the presence of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery...
The Issue: Unit Defect: Firm inspection revealed units did not have the compartment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit Recalled by...
The Issue: Disengaged screw head could potentially not be retained in the Torque...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT Recalled...
The Issue: Toshiba American Medical Systems (TAMS) is recalling the Aquilion CT system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OR Table Recalled by Trumpf Medical Systems, Inc. Due to Trumpf has...
The Issue: Trumpf has identified six incidents of pinched cables.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UROPHEN MB URINARY ANTISEPTIC Tablets Recalled by Burel Pharmaceuticals Inc...
The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UROLET MB URINARY ANTISEPTIC Recalled by Burel Pharmaceuticals Inc Due to...
The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.