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. 1,065 recalls have been distributed to Nebraska in the last 12 months.
Showing 15781–15800 of 49,150 recalls
Recalled Item: Tranberg MR Stylet Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Wheelchair Recalled by Merits Holdings Co. dba Merits Health Products,...
The Issue: Seat baseplate pin has broken in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DirectInject consists of a sterile dual paste system which is Recalled by...
The Issue: Inability for the user to inject the paste from the syringe into the target...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Itraconazole Capsules Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Burro en Primavera Recalled by QMart Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PremierZen Extreme 3000 Recalled by QMart Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Guanfacine Extended-Release Tablets 2 mg Recalled by Apotex Corp. Due to...
The Issue: Cross Contamination with Other Product: Product is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMPERIAL GOLD 2000 Recalled by QMart Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imperial Platinum 2000 Recalled by QMart Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Riomet (metformin hydrochloride oral solution) 500 mg/5 mL Cherry Flavor...
The Issue: Microbial Contamination of Non-Sterile Product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medex 10 IN Pressure Injector Line w/Rot (1200psi) NS. Recalled by Smiths...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH PRESSURE TUBING Recalled by Smiths Medical ASD Inc. Due to Specific...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH PRESSURE ROTATOR (Component) a. WITH MALE LUER LOCK Recalled by Smiths...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gang Cath Lab Set Recalled by Smiths Medical ASD Inc. Due to Specific lots...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surveyor S12/S19 Bedside Patient Monitor Recalled by Welch Allyn Inc Mortara...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR Recalled by...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AM12M Acquisition Module accessory. Impacted software version of the AM12M...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LogiCal Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LogiCal Monitoring Set Recalled by Smiths Medical ASD Inc. Due to Specific...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stopcock rotator (Component): a. 1050 STOPCOCK ROTATOR Recalled by Smiths...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.