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. 2,579 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,579 in last 12 months

Showing 881900 of 49,311 recalls

FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Green Maeng Da powder is packaged in Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom White Elephant powder is packaged in seal Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Red Bali powder is packaged in seal Recalled by Lotus...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Bali Gold powder is packaged in seal Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 30, 2025· Cepheid

Recalled Item: Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-10 Recalled...

The Issue: Invitro diagnostic test kits with specimens that have elevated white blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2025· Cepheid

Recalled Item: Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10...

The Issue: Invitro diagnostic test kits with specimens that have elevated white blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Medicrea International

Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...

The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...

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

Class II — Potential Health HazardOngoing
DrugOctober 29, 2025· Otsuka ICU Medical LLC

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 29, 2025· Otsuka ICU Medical LLC

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 29, 2025· Medicrea International

Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...

The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Copan Italia

Recalled Item: 1ml of DTT in liquid phase Recalled by Copan Italia Due to Treatment reagent...

The Issue: Treatment reagent functionality in respiratory specimens liquification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Copan Italia

Recalled Item: 1ml of DTT in liquid phase Recalled by Copan Italia Due to Treatment reagent...

The Issue: Treatment reagent functionality in respiratory specimens fluidification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Philips North America Llc

Recalled Item: CT 5300 Recalled by Philips North America Llc Due to If the screws of tube...

The Issue: If the screws of tube heat exchanger on the rotating scanner are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Philips North America Llc

Recalled Item: Incisive CT Recalled by Philips North America Llc Due to If the screws of...

The Issue: If the screws of tube heat exchanger on the rotating scanner are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Medtronic, Inc.

Recalled Item: Aurora EV-ICD and Clinical EV-ICD Recalled by Medtronic, Inc. Due to There...

The Issue: There is a potential for delayed time to high-voltage (HV) therapy should a...

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

Class II — Potential Health HazardOngoing
DrugOctober 28, 2025· Agebox

Recalled Item: Agebox iKids-Growth (Night Formula) Recalled by Agebox Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· Agebox

Recalled Item: Agebox iKids-Growth (Day Formula) capsules Recalled by Agebox Due to...

The Issue: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund