Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 955 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
955 in last 12 months

Showing 34861–34880 of 47,938 recalls

Medical DeviceNovember 13, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Optima CL323i Product Usage: The angiographic X-ray systems...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet HCU 30 Coolant Type R134A Filling weight 250 g Recalled by Maquet...

The Issue: Failure of the HEATER-COOLER UNIT (HCU 30) Type 2 power supply board. A drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2015· STERILMED, INC.

Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Sterilmed, Inc. is voluntarily...

The Issue: Sterilmed, Inc. is voluntarily recalling all unexpired Reprocessed...

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

Class II — Potential Health HazardOngoing
FoodNovember 13, 2015· A. L. Schutzman Company, Inc.

Recalled Item: Honey Mustard Mix sold under the following brand: Ashdon Farms Recalled by...

The Issue: The honey mustard mix lists whey in the ingredient list but does not list...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 13, 2015· A. L. Schutzman Company, Inc.

Recalled Item: Honey Mustard Pretzel Mix sold under the following brand and size: Girl...

The Issue: The honey mustard pretzel mix lists whey in the ingredient list but does not...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 12, 2015· Trader Joes Company

Recalled Item: Butternut Squash Triangoli Recalled by Trader Joes Company Due to Undeclared...

The Issue: Trader Joe's is recalling Trader Giotto's Butternut Squash Triangoli because...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038 Post-Operative...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 Post-Operative...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Bestmed, LLC

Recalled Item: Digital Temple Thermometer labeled under: Bestmed Recalled by Bestmed, LLC...

The Issue: An incorrect calibration of the thermometer that causes the device to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011 Post-Operative...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: ADV ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-231...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

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

Class II — Potential Health HazardOngoing
DrugNovember 12, 2015· Teva Pharmaceuticals USA

Recalled Item: DEXTROAMPHETAMINE SACCHARATE Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications: High out of specification test...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· ConvaTec, Inc

Recalled Item: Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended...

The Issue: The Nebulizer mask malfunctions in that there is reduced or no aerosol...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care pBNP TestPak- in vitro diagnostic test for Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing