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. 2,612 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,612 in last 12 months

Showing 86418660 of 13,356 recalls

DrugSeptember 15, 2016· Pfizer Inc.

Recalled Item: PREMARIN (conjugated estrogen tablets Recalled by Pfizer Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Bottles were incorrectly...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 13, 2016· Teva Pharmaceuticals USA

Recalled Item: mitoXANTRONE Injection USP (concentrate) Recalled by Teva Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: potential failure to meet the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 13, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2016· Pfizer Inc.

Recalled Item: Cytotec (misoprostol) Tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradations Specifications; Out of specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 8, 2016· Mckesson Packaging Services

Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Mckesson Packaging...

The Issue: Labeling: Label mix-up. The inner packaging was properly labeled Omeprazole...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 8, 2016· Novo Nordisk Inc

Recalled Item: GlucaGen HypoKit (glucagon [rDNA origin] for injection) Recalled by Novo...

The Issue: Defective delivery system: detached needles on the syringe in the kit.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 7, 2016· Biocompatibles U.K., Ltd.

Recalled Item: Varithena (polidocanol injectable foam) Administration Pack For Use With...

The Issue: Defective Delivery System: Incorrect type of syringe found in commercially...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 2, 2016· Shire

Recalled Item: Vyvanse (lisdexamfetamine dimesylate) Capsules 30 mg Recalled by Shire Due...

The Issue: Presence of Foreign Tablets/Capsules

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 2, 2016· United Exchange Corporation

Recalled Item: Eye Wash Recalled by United Exchange Corporation Due to Lack of assurance of...

The Issue: Lack of assurance of sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 2, 2016· United Exchange Corporation

Recalled Item: Eye Irrigating Solution Recalled by United Exchange Corporation Due to Lack...

The Issue: Lack of assurance of sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 2, 2016· United Exchange Corporation

Recalled Item: EYE WASH Recalled by United Exchange Corporation Due to Lack of assurance of...

The Issue: Lack of assurance of sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 2, 2016· United Exchange Corporation

Recalled Item: EYE WASH Recalled by United Exchange Corporation Due to Non-Sterility:...

The Issue: Non-Sterility: Direct evidence of contamination for 2 lots based on FDA samples.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 2, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Hyoscyamine Sulfate Recalled by VIRTUS PHARMACEUTICALS OPCO II L Due to...

The Issue: Failed Content Uniformity Specifications: resulting in both superpotent and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 2, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Hyoscyamine Sulfate Recalled by VIRTUS PHARMACEUTICALS OPCO II L Due to...

The Issue: Failed Content Uniformity Specifications: resulting in both superpotent and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 2, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Hyoscyamine Sulfate Recalled by VIRTUS PHARMACEUTICALS OPCO II L Due to...

The Issue: Failed Content Uniformity Specifications: resulting in both superpotent and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 30, 2016· Actavis Laboratories, FL, Inc.

Recalled Item: Ramipril Capsules Recalled by Actavis Laboratories, FL, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugAugust 29, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: ZENATANE (isotretinoin capsules USP) 20 mg Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund