Product Recalls in New Hampshire

Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,367 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,367 in last 12 months

Showing 2698127000 of 49,311 recalls

FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Raisins Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Pretzel Balls Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Coconut Bites Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Strawberries Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Powerberry Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Peanuts Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Cashews Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Ginger Snap Cookies Recalled by GKI Foods, LLC Due to...

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Cherries Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 26, 2017· ConvaTec, Inc

Recalled Item: SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible...

The Issue: A portion of Lot 7H02242 outer boxes (market units) of the SUR-FIT Natura...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Arterial Access Tray Recalled by Arrow International Inc Due to The povidone...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
DrugOctober 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Dutasteride and Tamsulosin HCl Capsules Recalled by Teva Pharmaceuticals USA...

The Issue: Failed dissolution specifications; all lots within expiry are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2017· Fagron, Inc

Recalled Item: Estriol Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...

The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2017· Amerisource Health Services

Recalled Item: Paroxetine Tablets Recalled by Amerisource Health Services Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules.

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

Class II — Potential Health HazardOngoing
Refund