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. 2,400 recalls have been distributed to Nebraska in the last 12 months.
Showing 36941–36960 of 49,150 recalls
Recalled Item: 18inch Dual Port/Single Bladder Disposable Tourniquet Cuff Recalled by...
The Issue: The inside of the folded Instructions For Use (IFU) pamphlet was missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical P-440 Portable Ceiling Lift Recalled by ErgoSafe Products, LLC...
The Issue: There is a potential the sling loops may not stay attached to the carry bar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Desmopressin Acetate Tablets Recalled by Actavis Laboratories, FL, Inc. Due...
The Issue: Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: O-Two Adult Ventilation Timer Recalled by O-Two Medical Technologies, Inc....
The Issue: Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to the...
The Issue: the Fabius MRI or parts of the system were attracted by the magnetic field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abutment Retrieval Instrument Zirconia CC RP/WP Recalled by Nobel Biocare...
The Issue: One dimension of the affected instrument is incorrect. Therefore this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems with software versions...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Milex Vaginal-Hymenal Silicone Dilators Set of 4 P/N MX20 Product Recalled...
The Issue: Incorrect expiration date on outer carton kit label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sour Caramel Apple Chewing Recalled by Project 7 Due to Undeclared Milk
The Issue: Project 7 is recalling all lots of Sour Caramel Apple Chewing Gum because...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Disulfiram tablets Recalled by Qualitest Pharmaceuticals Due to Failed...
The Issue: Failed Dissolution Specifications: During routine stability testing at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Invivo Expression MRI Patient Monitoring System. Recalled by Philips...
The Issue: The device's labeling inaccurately indicates Endotracheal as a body...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mission -Breath Alcohol Detector -15 tests - 0.08% BAC - Recalled by Acon...
The Issue: Acon Laboratories, Inc. is recalling Mission Breath Alcohol Detector due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSTRUMENT ARM DRAPE Recalled by Intuitive Surgical, Inc. Due to Field...
The Issue: Field Safety Notification to advise of an issue that may occur involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Potential colonization of organisms, including Mycobacteria, in Sorin Heater...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.