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. 2,547 recalls have been distributed to North Dakota in the last 12 months.
Showing 5741–5760 of 47,938 recalls
Recalled Item: Sammy's Milk GOAT MILK TODDLER FORMULA Recalled by Graceleigh, Inc. dba...
The Issue: FDA inspection and investigation of firm's website and social media pages...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sammy's Milk GOAT MILK TODDLER FORMULA Recalled by Graceleigh, Inc. dba...
The Issue: FDA inspection and investigation of firm's website and social media pages...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Synchro2 Guidewires are a steerable guidewire family with a Recalled by...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Recalled by BD...
The Issue: Due to infusion set tubing drip chamber becoming detached from the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro SELECT Guidewires are a steerable guidewire family with Recalled...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro Neuro Guidewires are a steerable guidewire family with Recalled...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES 4000 Hysteroscope Recalled by Olympus Corporation of the Americas Due to...
The Issue: The required leakage test was not performed following of a re-work for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG:...
The Issue: Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optum Nimbus II Plus Recalled by OptumHealth Care Solutions LLC Due to...
The Issue: Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bull Frog SPF 50 Amphibious Lotion SPF 50 Amphibious Lotion Recalled by ARG...
The Issue: Out of Specification for active ingredient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.