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. 2,436 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,436 in last 12 months

Showing 3072130740 of 49,150 recalls

FoodJanuary 12, 2017· Hy-Vee Stores Inc

Recalled Item: Holiday Candy packaged in a 10"/16oz. () Recalled by Hy-Vee Stores Inc Due...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 12, 2017· Hy-Vee Stores Inc

Recalled Item: Peppermint Bark packaged in 4oz. () Recalled by Hy-Vee Stores Inc Due to...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 12, 2017· Hy-Vee Stores Inc

Recalled Item: Dazzled Peanut Brittle packaged in 8oz. () and 12 Recalled by Hy-Vee Stores...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 12, 2017· Vascular Solutions, Inc.

Recalled Item: GrebSet Micro-Introducer Kit Recalled by Vascular Solutions, Inc. Due to...

The Issue: Four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Monitor Recalled by Physio-Control, Inc. Due to The firm has...

The Issue: The firm has become aware of a potential device issue where the LIFEPAK 15...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 12, 2017· Carestream Health Inc

Recalled Item: Carestream DRX-Revolution Mobile X-Ray System Recalled by Carestream Health...

The Issue: The firm received a complaint alleging that a DRX Revolution System could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2017· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to There is...

The Issue: There is a potential for radio frequency (RF) interference to alter wireless...

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

Class II — Potential Health HazardOngoing
FoodJanuary 11, 2017· Weaver Popcorn Co.

Recalled Item: Trail's End Chicago Cubs Sweet and Savory Collection Trail's End Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 11, 2017· Robert Rothschild Farm LLC

Recalled Item: Gift Sets with Chocolate Pretzel Dippers Recalled by Robert Rothschild Farm...

The Issue: The product is not labeled with an ingredient statement and therefore, does...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 11, 2017· Robert Rothschild Farm LLC

Recalled Item: Gift Sets with Pretzel Twists Recalled by Robert Rothschild Farm LLC Due to...

The Issue: The product is not labeled with an ingredient statement and therefore, does...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 11, 2017· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a Recalled...

The Issue: Ortho Kinematics Inc. sent a Notice of Correction to Released Testing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Kiscomedica S.A.

Recalled Item: L-Varlock Cage/Trial Implant Holder Recalled by Kiscomedica S.A. Due to Firm...

The Issue: Firm received a complaint of the tip holder breaking during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Open Procedure Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Nasal Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Ortho Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Upper Torso Tray Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Minor/General/Ortho Pack Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Surgical Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Major Pack (1345) Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing