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. 1,036 recalls have been distributed to North Dakota in the last 12 months.
Showing 14201–14220 of 47,938 recalls
Recalled Item: LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray Recalled...
The Issue: cGMP Deviations: LOTRIMIN AF (Tolnaftate 1%) manufactured at the same...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can Recalled by...
The Issue: cGMP Deviations: manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tinactin (Tolnaftate 1%) JOCK ITCH POWDER SPRAY NET WT133g (4.6 oz) can...
The Issue: Chemical Contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NOW Ginseng & Royal Jelly 90 VCAPS MMA Recalled by NOW Health Group Inc. Due...
The Issue: Product may contain Metronidazole
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NOW Bee Pollen 500mg 100 VCAPS Recalled by NOW Health Group Inc. Due to...
The Issue: Product may contain Metronidazole
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pharmanex Kids Jungamals Recalled by NSE Products, Inc. Due to Pharmanex...
The Issue: Pharmanex Jungamals was found to have a missing fish allergen statement on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NOW Royal Jelly 1500mg 60 VCAPS NOW Royal Recalled by NOW Health Group Inc....
The Issue: Product may contain Metronidazole
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coppertone SPORT Sunscreen Spray 50 Recalled by Beiersdorf Inc Due to...
The Issue: Chemical contamination; presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide...
The Issue: Chemical contamination; presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide...
The Issue: Chemical contamination; presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coppertone SPORT MINERAL 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%...
The Issue: Chemical contamination; presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%...
The Issue: Chemical contamination; presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MENTOR Saline-Filled Breast Implants are constructed from room temperature...
The Issue: Due to a manufacturing issue, Implant may have a potentially weakened area...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.