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. 2,491 recalls have been distributed to Nebraska in the last 12 months.
Showing 18241–18260 of 49,150 recalls
Recalled Item: CMExpress Microbore Sets Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMExpress Microbore Set Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset with Filter Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset With Female Luer Recalled by CME America, LLC Due to...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset with Filter Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMExpress Microbore Set Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Recalled by...
The Issue: Convenience kit mislabeled with the incorrect catheter effective length on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP with assay: Luminex Recalled by Luminex Corporation...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP with assay Luminex Recalled by Luminex Corporation Due...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tropical Lip Moisturizer Recalled by Yusef Manufacturing Laboratories, LLC...
The Issue: Superpotent Drug: The beginning portion of the batch appears to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by The Harvard...
The Issue: CGMP Deviation: Potential presence of Nitrosodimethylamine (NDMA) Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.