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. 1,065 recalls have been distributed to North Dakota in the last 12 months.
Showing 3401–3420 of 27,512 recalls
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barricaid Annular Closure Impactor Recalled by Intrinsic Therapeutics, Inc....
The Issue: At least two units have been found to be missing a weld.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivo 45 LS Recalled by Breas Medical, Inc. Due to There is a potential for...
The Issue: There is a potential for short term (<7 days) elevated levels of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 3.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 3.0mm Precision Match Head Recalled by Stryker Corporation Due...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 4.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 4.0mm Diamond Round Recalled by Stryker Corporation Due to...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 3.0mm Diamond Match Head Recalled by Stryker Corporation Due to...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 4.0mm Precision Round Recalled by Stryker Corporation Due to...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Syringe 60CC Recalled by Cypress Medical Products LLC Due to...
The Issue: Affected syringes lack FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 3.0mm Diamond Round Recalled by Stryker Corporation Due to...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.