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. 2,548 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,548 in last 12 months

Showing 1540115420 of 49,150 recalls

Medical DeviceMay 14, 2021· DeRoyal Industries Inc

Recalled Item: DeRoyal Angio Cath Removal Tray Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2021· DeRoyal Industries Inc

Recalled Item: DeRoyal Pacemaker Tray Pgybk Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2021· DeRoyal Industries Inc

Recalled Item: DeRoyal Heart Cath Procedure Pack Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2021· Smiths Medical ASD Inc.

Recalled Item: PORTEX UNLTRperc Percutaneous Dilation Tracheostomy Kit Recalled by Smiths...

The Issue: One lot number of a specific model of ULTRAperc Percutaneous Dilation...

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

Class II — Potential Health HazardOngoing
DrugMay 14, 2021· Teligent Pharma, Inc.

Recalled Item: Diflorasone Diacetate Ointment USP Recalled by Teligent Pharma, Inc. Due to...

The Issue: Presence of Foreign Substance: Foreign particles observed during routine...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 14, 2021· Medline Industries Inc

Recalled Item: READYPREP CHG Recalled by Medline Industries Inc Due to Superpotent Drug:...

The Issue: Superpotent Drug: Product is above specification for active ingredient, 2%...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer - multi-component system for in vitro Recalled by...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer - multi-component system for in vitro Recalled by...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: InTouch 2131-intended to support a human patient in an acute care setting...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: IsoGel Air - support surface assists in the prevention and Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: GoBed II MedSurg Bed Recalled by Stryker Medical Division of Stryker...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Proform- support surface is used to assist in the prevention Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Symmetry Plus Treatment Recliner - general hospital use as a Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: ComfortGel - assists in the prevention and treatment of all Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Encore Medical, LP

Recalled Item: DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus Recalled by Encore...

The Issue: Packaging mixup; There is a potential that packaging identified as 12mm knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· W L Gore & Associates, Inc.

Recalled Item: Gore Propaten Vascular Graft configured for Pediatric Shunt Recalled by W L...

The Issue: Vascular Grafts containing an inner diameter of 6 mm may be incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...

The Issue: Labeling does not include guidance for proper water-quality maintenance and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Stretcher Chair-for use in all acute care hospitals and medical Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing