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. 1,069 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
1,069 in last 12 months

Showing 13521–13540 of 49,150 recalls

FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: Dole 13oz Southwest Kit SKU: 2776 Recalled by Dole Fresh Vegetables Inc Due...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: Kroger 12 oz American Blend SKU: 3003 Recalled by Dole Fresh Vegetables Inc...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 5, 2022· Becton Dickinson & Co.

Recalled Item: BD Veritor Plus Analyzer - intended to provide rapid test Recalled by Becton...

The Issue: May have the potential to overheat and/or cause fire, the issue can occur...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2022· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as Recalled by...

The Issue: May have adhesive residue on the posterior surface of the femoral augment,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2022· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Recalled...

The Issue: May have adhesive residue on the posterior surface of the femoral augment,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 5, 2022· Akorn, Inc.

Recalled Item: Sufentanil Citrate Injection Recalled by Akorn, Inc. Due to Subpotent Drug:...

The Issue: Subpotent Drug: Out of specification for assay at the 30-month stability...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Semglee (insulin glargine) injection Recalled by Mylan Pharmaceuticals Inc...

The Issue: Labeling: Missing Label: label missing from some Semglee prefilled pens.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Rite Aid Pharmacy Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Kroger Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Leader Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddys Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Wal-Fex D Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Rugby Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: equate Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: CVS Health Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: QC QUALITY CHOICE Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 4, 2022· BALT USA, LLC

Recalled Item: The Optima Coil System consists of an implantable embolization coil Recalled...

The Issue: Due to Label/Pouch mix-up. Pouches incorrectly labeled. Incorrect shelf...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2022· Smith & Nephew, Inc.

Recalled Item: INTEGRA SURFIX ALPHA Screwdriver Torx 10 Recalled by Smith & Nephew, Inc....

The Issue: The affected screwdrivers are out of specification and may not mate with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2022· Philips North America Llc

Recalled Item: eCareManager version 4.2.1 Recalled by Philips North America Llc Due to...

The Issue: eCareManager (eCM) Sentry Score software not approved for use

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2022· Immuno-Mycologics, Inc

Recalled Item: CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY Recalled by Immuno-Mycologics, Inc...

The Issue: The firm found immunoassay products used to detect cryptococcal antigen in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing