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. 2,535 recalls have been distributed to North Dakota in the last 12 months.
Showing 9001–9020 of 47,938 recalls
Recalled Item: bellavista 1000e Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...
The Issue: Vyaire Medical identified two patient safety risks during the use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bellavista 1000 Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...
The Issue: Vyaire Medical identified two patient safety risks during the use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betta Link LG Reusable Fishmouth Guide-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK SR REUSABLE PRONGED GUIDE- Intended for use in Recalled by T.A.G....
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK LG KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betta Link LG Reusable ProngED Guide - Intended for use Recalled by T.A.G....
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165 CM 10/BX- Intended Recalled...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165CM 5/BX- Intended for...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 230 CM 10/BX- Intended Recalled...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 230CM 5/BX- Intended for...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine Sublingual Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pin-Away PYRENTAL PAMOATE (Pyrantel base 50 mg / mL) Pinworm Treatment...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safe tussin PM Recalled by Denison Pharmaceuticals, LLC Due to CGMP...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colic Calm Recalled by Denison Pharmaceuticals, LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safe tussin DM Recalled by Denison Pharmaceuticals, LLC Due to CGMP...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gose con Sandia Recalled by Avery Brewing Company Due to Due to over...
The Issue: Due to over pressurization, can may fail/explode.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MEDLINE THERAHONEY GEL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline issued a recall on TheraHoney Wound Gel due to the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to Device...
The Issue: Device may experience malfunctions due to misalignment of the check valve in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.