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. 2,510 recalls have been distributed to North Dakota in the last 12 months.
Showing 13341–13360 of 13,369 recalls
Recalled Item: Man King Capsules Recalled by www.vitaminbestbuy.com Due to Marketed Without...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hard Ten Days Capsule Recalled by www.vitaminbestbuy.com Due to Marketed...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Japan Weight Loss Blue Capsules Recalled by www.vitaminbestbuy.com Due to...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sibutramine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL injection Recalled by...
The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL Injection Recalled by...
The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.050mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Actra-SX 500 Capsules Recalled by Body Basics Inc Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA; product contains sildenafil, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep with Tint Recalled by Carefusion 213, Llc Due to Lack of...
The Issue: Lack of Assurance of Sterility: A customer complaint reported some units had...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prefera OB One Gel Capsules Recalled by Meda Pharmaceuticals Inc. Due to...
The Issue: Labeling: Presence of Undeclared Color Additive; The product is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xactdose Phenytoin Oral Suspension Recalled by VistaPharm, Inc. Due to...
The Issue: Defective container; lidding deformity allows the contained product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Murocel (methylcellulose) Lubricant Opthalmic Solution (USP Recalled by...
The Issue: Lack of Assurance of Sterility: Bausch & Lomb, Inc. is recalling 7 Lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Nasal Solution Recalled by Apotex Corp. Due to CGMP...
The Issue: CGMP Deviations: tubing used for filling may interact with the nasal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PIRACETAM COGNITION ENHANCING AGENT Dietary Supplement PHARMACEUTICAL GRADE...
The Issue: Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PIRACETAM POWDER COGNITION ENHANCING AGENT Dietary Supplement CTD 500 grams...
The Issue: Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.