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. 2,480 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,480 in last 12 months

Showing 1988119900 of 49,150 recalls

Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: MICRO-PSD Electron Recalled by Angiodynamics, Inc. Due to May result in...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: MICRO-PSD EXTERNAL BEAM PHOTON Recalled by Angiodynamics, Inc. Due to May...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system Recalled by...

The Issue: Editing a static arc beam may unexpectedly set the MU of the beam to its...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Leica Microsystems, Inc.

Recalled Item: BOND Polymer Detection Kit Recalled by Leica Microsystems, Inc. Due to BOND...

The Issue: BOND Polymer Detection kits (DS9800) were held out of storage longer than...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Boston Scientific Corporation

Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...

The Issue: During testing on the Habib EUS RFA device, a temperature increase was...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Boston Scientific Corporation

Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...

The Issue: During testing on the Habib EUS RFA device, a temperature increase was...

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

Class II — Potential Health HazardOngoing
DrugNovember 15, 2019· Rising Pharmaceuticals, Inc.

Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...

The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Rising Pharmaceuticals, Inc.

Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...

The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Grato Holdings, Inc.

Recalled Item: Colostat Recalled by Grato Holdings, Inc. Due to Labeling mix-up -...

The Issue: Labeling mix-up - Indications on product label are incorrect.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Akorn, Inc.

Recalled Item: MYORISAN (isotretinoin capsules Recalled by Akorn, Inc. Due to Unit Dose...

The Issue: Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 15, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clobetasol Propionate Foam Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Defective delivery system; product is not foaming or is coming out as liquid.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation) Recalled by Glenmark...

The Issue: Defective delivery system; product is not foaming or is coming out as liquid.

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

Class III — Low RiskOngoing
Refund
FoodNovember 15, 2019· SARA LEE FROZEN FOODS

Recalled Item: Chef Pierre 37 Ounce Pumpkin Spice Latte Pie Recalled by SARA LEE FROZEN...

The Issue: undeclared FD & C Red 40

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

Class III — Low RiskOngoing
Refund
FoodNovember 15, 2019· THE KRAFT HEINZ COMPANY

Recalled Item: Breakstones 4% Milkfat Small Curd Cottage Cheese Recalled by THE KRAFT HEINZ...

The Issue: Potential presence of pieces of red plastic and metal that may have been...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 15, 2019· THE KRAFT HEINZ COMPANY

Recalled Item: Breakstones 4% Milkfat Large Curd Cottage Cheese Recalled by THE KRAFT HEINZ...

The Issue: Potential presence of pieces of red plastic and metal that may have been...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 15, 2019· THE KRAFT HEINZ COMPANY

Recalled Item: Breakstones 2% Milkfat Lowfat Large Curd Cottage Cheese Recalled by THE...

The Issue: Potential presence of pieces of red plastic and metal that may have been...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 15, 2019· Baxter Healthcare Corporation

Recalled Item: Revaclear Capillary Dialyzer 300 Recalled by Baxter Healthcare Corporation...

The Issue: There is the potential presence of particular matter in the header caps of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2019· Tytek Medical Inc

Recalled Item: PneumoDart Recalled by Tytek Medical Inc Due to A defect involving an...

The Issue: A defect involving an occluded needle was discovered during a training exercise.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2019· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm" O2 Imaging System Recalled by Medtronic Navigation, Inc.-Littleton...

The Issue: Due to a manufacturing issue affecting particular O-arm" O2 Imaging Systems,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2019· Tosoh Smd Inc

Recalled Item: AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment...

The Issue: The AIA-2000 bar code scanners depend on the quiet zone to help identify the...

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

Class III — Low RiskOngoing