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. 2,573 recalls have been distributed to North Dakota in the last 12 months.
Showing 1341–1360 of 47,938 recalls
Recalled Item: ICU Medical ChemoLock w/Mini Bag Spike ¿ Recalled by ICU Medical, Inc. Due...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Oncology Kit w/31" (79 cm) 20 Drop Admin Recalled by ICU...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical 7.5" (19 cm) Appx 1.5 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical ChemoLock Bag Spike with Clave Additive Port Recalled by ICU...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical ChemoLock Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoLock Bag Spike Recalled by ICU Medical, Inc. Due to Port weld of drug...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical 60" (152 cm) Appx 1.2 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical ChemoLock Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical ChemoLock Universal Vented Vial Spike Recalled by ICU Medical,...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300....
The Issue: Potential for compromised integrity of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120....
The Issue: Potential for compromised integrity of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everolimus tablets 5mg Recalled by Endo USA, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution Recalled by Apotex...
The Issue: Lack of Assurance of Sterility; atypical weight loss due to improper bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Apotex Corp. Due to...
The Issue: Lack of Assurance of Sterility; atypical weight loss due to improper bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclophosphamide Injection 500 mg/5 mL (100 mg/mL) Recalled by Sandoz Inc...
The Issue: cGMP deviations: Temperature excursion during transportation.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...
The Issue: Due to display cables used for monitors were not in compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...
The Issue: Due to display cables used for monitors were not in compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...
The Issue: Due to display cables used for monitors were not in compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Re-Direction Endoluminal Devices: FRED 27 Recalled by MICROVENTION INC....
The Issue: Flow diverter may have a manufacturing issue related to the tantalum length...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW Server 2.0 Recalled by GE Medical Systems, SCS Due to Firm has identified...
The Issue: Firm has identified a security vulnerability in AW Server products. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.