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. 902 recalls have been distributed to North Dakota in the last 12 months.
Showing 47321–47340 of 47,938 recalls
Recalled Item: CPB CATHETER KIT-DR BARTLES Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien ROTICULATOR 55-4.8 Single Use Stapler REF# 017614 The RETICULA...
The Issue: Potential for the sterility barrier to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM CPB CATHETER KIT-DR. Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 14-GAUGE...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dent's Extra Strength Toothache Gum Recalled by Grandpa Brands Co Due to...
The Issue: Superpotent; benzocaine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morton Recalled by Morton Salt Co. Due to Impurities/Degradation Products:...
The Issue: Impurities/Degradation Products: The product was found to contain a slightly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Recalled by Hill...
The Issue: Subpotent; fluocinolone acetonide
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Topical Oil (Scalp Oil)...
The Issue: Subpotent; fluocinolone acetonide
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12...
The Issue: Siemens Healthcare Diagnostics has confirmed that the presence of Intrinsic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panera Recalled by Panera Bread LLC Due to Product ingredient statement...
The Issue: Product ingredient statement reversed for Reduced Fat Honey Walnut Cream...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen Salted Clam Recalled by Seoul Shik Poom, Inc. Due to Korean Certified...
The Issue: Korean Certified Shippers delisted from ICSSL.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen Oysters Recalled by Seoul Shik Poom, Inc. Due to Korean Certified...
The Issue: Korean Certified Shippers delisted from ICSSL.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Panera HONEY WALNUT CREAM CHEESE SPREAD Recalled by Panera Bread LLC Due to...
The Issue: Product ingredient statement reversed for Reduced Fat Honey Walnut Cream...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human...
The Issue: The Beauty Angel was marketed without a 510k.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USA-002 Rev A brochure is a two sided tri-fold printed Recalled by...
The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V Series Patient Monitors Recalled by Mindray DS USA, Inc. d.b.a. Mindray...
The Issue: Mindray has identified two software anomalies contained in the V Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US-001 Rev A brochure is a two sided tri-fold printed Recalled by...
The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endocet (oxycodone and acetaminophen) tablets Recalled by Endo...
The Issue: Adulterated Presence of Foreign Tablets: Customer complaint that some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products Recalled by...
The Issue: Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.