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. 955 recalls have been distributed to North Dakota in the last 12 months.
Showing 32381–32400 of 47,938 recalls
Recalled Item: VITROS Immunodiagnostic Products Total T4 Reagent Pack Recalled by...
The Issue: Ortho-Clinical Diagnostics confirmed that sample results generated from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parker Trach-Vac Endotracheal Tubes. Tyvek pouches Recalled by Parker...
The Issue: Parker Medical announces a voluntary field action for the Parker Trach-Vac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quaker quinoa granola bars Recalled by The Quaker Oats Company Due to...
The Issue: SunOpta expanded their recall of listeria Monocytogenes in sunflower...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Quaker Quinoa Granola Bars Recalled by The Quaker Oats Company Due to...
The Issue: SunOpta expanded their recall of listeria Monocytogenes in sunflower...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Urea (50% Urea in a Cream Base) Recalled by Exact-Rx Inc Due to...
The Issue: Crystallization; complaints received by the manufacturer of crystals forming...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHLORHEXIDINE GLUCO. 0.12% ORAL RINSE Recalled by Aidarex Pharmaceuticals...
The Issue: Failed Impurity/Degradation Specifications: Out of specifications for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin OPTH 0.3% SOL Recalled by Aidarex Pharmaceuticals LLC Due to...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: mitoXANTRONE Injection USP (concentrate) Recalled by Teva North America Due...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Part # 313.211 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...
The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #313.231 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...
The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Video Bronchoscope Designed to be used with a Pentax Recalled by...
The Issue: Pentax America Inc. is recalling various bronchoscopes which contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part # 313.212 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...
The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Ti Button Plate 7 Holes Recalled by Synthes (USA) Products LLC Due...
The Issue: DePuy Synthes is voluntarily initiating a recall due to affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Video Bronchoscope The EB-1970UK Recalled by Pentax of America...
The Issue: The EB-1970UK Ultrasound Video Bronchoscope shipped between the clearance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part # SD313.012 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...
The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #313.221 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...
The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part # 313.946 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...
The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part # 313.232 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...
The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part # SD313.011 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...
The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxylog 3000 Recalled by Draeger Medical, Inc. Due to Isolated episodes of...
The Issue: Isolated episodes of leakage at the check valve were found
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.