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. 2,553 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,553 in last 12 months

Showing 52215240 of 47,938 recalls

FoodJune 13, 2024· Totally Cool, Inc.

Recalled Item: Dolcezza Peanut Butter Stracciatella Gelato 16 fl oz/1 pint Recalled by...

The Issue: Possible contamination with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2024· Totally Cool, Inc.

Recalled Item: Marco Turkish Mocha Ice Cream 16 fl oz/1 pint Recalled by Totally Cool, Inc....

The Issue: Possible contamination with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2024· PACIRA PHARMACEUTICALS INC

Recalled Item: Zilretta (triamcinolone acetonide extended-release injectable suspension)...

The Issue: Failed Dissolution Specifications - did not meet the acceptance criteria for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 12, 2024· Synergetics Inc

Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...

The Issue: Sterilization certificates could not be validated by the supplier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2024· Synergetics Inc

Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...

The Issue: Sterilization certificates could not be validated by the supplier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2024· Synergetics Inc

Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...

The Issue: Sterilization certificates could not be validated by the supplier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2024· Synergetics Inc

Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...

The Issue: Sterilization certificates could not be validated by the supplier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2024· Boston Scientific Corporation

Recalled Item: Autotome RX 20mm CUT WIRE Cannulating Sphincterotome Recalled by Boston...

The Issue: Foreign material may be present on the enclosed section of the cutting wire...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Medical Action Industries, Inc. 306

Recalled Item: Foam Protective Pouches Recalled by Medical Action Industries, Inc. 306 Due...

The Issue: The protective pouches were identified to have been improperly labeled with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Ethicon Sarl, a Johnson & Johnson Company

Recalled Item: SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM) Recalled by Ethicon Sarl, a Johnson...

The Issue: Some foil pouches were found torn open, impacting the sterile barrier which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing