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. 2,617 recalls have been distributed to Nebraska in the last 12 months.
Showing 6601–6620 of 49,150 recalls
Recalled Item: Acthar Gel (repository corticotropin injection) 400 USP units/5mL (80 USP...
The Issue: cGMP deviations: Temperature excursion due to shipping delay from...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Terlivaz (terlipressin for injection) Recalled by Mallinckrodt Hospital...
The Issue: cGMP deviations: Temperature excursion due to shipping delay from...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arize Herbal Dietary Supplement Recalled by Today The World Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SCHWINNNG Herbal Dietary Supplement Recalled by Today The World Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sustain Herbal Dietary Supplement Recalled by Today The World Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 3 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 7 9 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 11 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 with a Certeray generator-To perform image guidance in diagnostic...
The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 with a Certeray generator -To perform image guidance in diagnostic...
The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 with a Certeray generator-To perform image guidance in diagnostic...
The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.