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 661680 of 49,311 recalls

FoodNovember 13, 2025· Jeni's Splendid Ice Creams LLC

Recalled Item: Jeni's Passion Fruit Dreamsicle Ice Cream Bars Recalled by Jeni's Splendid...

The Issue: Undeclared allergens - wheat and soy

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 13, 2025· Medline Industries, LP

Recalled Item: SCISSORS Recalled by Medline Industries, LP Due to The items may have weak...

The Issue: The items may have weak packaging seals that may result in a breach of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medline Industries, LP

Recalled Item: FORCEP Recalled by Medline Industries, LP Due to The items may have weak...

The Issue: The items may have weak packaging seals that may result in a breach of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medtronic MiniMed, Inc.

Recalled Item: InPen App Recalled by Medtronic MiniMed, Inc. Due to When app is uninstalled...

The Issue: When app is uninstalled and reinstalled, insulin pen software issue causes...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Abbott Laboratories

Recalled Item: Alinity ci-series System Control Module (SCM) Recalled by Abbott...

The Issue: Abbott Laboratories is recalling their Alinity ci-series System Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2025· Howmedica Osteonics Corp.

Recalled Item: The Stryker CranialMask Tracker is a single-use device consisting of...

The Issue: When the device is activated during surgery, the device software issues an...

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

Class II — Potential Health HazardOngoing
FoodNovember 12, 2025· Genepro Protein, Inc.

Recalled Item: Genepro Whey 4th Generation Plasma Treated Protein Recalled by Genepro...

The Issue: Product is mislabeled - the labeling contains incorrect ingredient...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 12, 2025· Medical Products Laboratories, Inc.

Recalled Item: Walgreens Saline Nasal Spray WITH XYLITOL Recalled by Medical Products...

The Issue: Microbial contamination of a non-sterile product - microorganism found to be...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 12, 2025· Remel, Inc

Recalled Item: 1. CAMHB W/LHB Recalled by Remel, Inc Due to Products may contain...

The Issue: Products may contain contamination, which may result in a darker or brown...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2025· Cardinal Health 200, LLC

Recalled Item: ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full...

The Issue: Affected gowns have the incorrect expiration date on the product packaging....

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

Class II — Potential Health HazardOngoing
DrugNovember 11, 2025· Dr. Reddy's Laboratories, Inc.

Recalled Item: Varenicline Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Sub...

The Issue: Sub potent drug: during the 9-month stability test conducted, the assay...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 11, 2025· AVID Medical, Inc.

Recalled Item: Halyard MINI PLUS KIT SOUTH Recalled by AVID Medical, Inc. Due to Devices...

The Issue: Devices are not suitable for organ transplant.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2025· AVID Medical, Inc.

Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...

The Issue: Devices are not suitable for organ transplant.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and Recalled...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic Recalled by...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

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

Class II — Potential Health HazardOngoing