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 3114131160 of 49,150 recalls

FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Condor Snacks Sour Cream & Onion W/O MSG. Product Code: T3235. 50 lb bags...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Jalapeno Popper Snack Seasoning / Shearer's Foods LLC. Product Code:...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Ranch Dressing / Hires Big H. Product Code: T3642. 500/14g pouch Recalled by...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Biscuits & Gravy Seasoning CR/ Barrel O' Fun. Product Code: T3669. 50 lb...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Super Otirod. Product Code: T3188. 50 lb bags Recalled by All American...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: White Cheddar Jalapeno Snack Seasoning / Barrel O' Fun. Product Recalled by...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Nacho Snack Seasoning / Harvest Pride /Tom Smith. Product Code: Recalled by...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Medacta Usa Inc

Recalled Item: Medacta International SA Recalled by Medacta Usa Inc Due to Damaged...

The Issue: Damaged packaging, lack of sterility assurance

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Tibial Component Fixed Hinge Small Long Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Cardiovascular Systems Inc

Recalled Item: DIAMONDBACK 360 Peripheral 1.50 Classic Recalled by Cardiovascular Systems...

The Issue: CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
DrugDecember 7, 2016· Novum Pharma, LLC

Recalled Item: Novacort Gel Sample Packets (2% hydrocortisone acetate Recalled by Novum...

The Issue: Subpotent Drug: Out of specification result for pramoxine hydrochloride

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 5, 2016· Acumed LLC

Recalled Item: OPT Croutons is a synthetic bone substitute designed for the Recalled by...

The Issue: OPT Croutons, part number 65-0210-S, is recalled due to the result of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System The product is used to manage Recalled by...

The Issue: Edits to Particle field definition parameters may not be saved when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...

The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...

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

Class I — Serious Health HazardOngoing