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. 2,292 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,292 in last 12 months

Showing 14211440 of 49,311 recalls

DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10/10 Product Codes: (1)722011 Recalled by PHILIPS MEDICAL...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/15 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Cardio Vascular-Allura Centron Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/15 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
DrugSeptember 2, 2025· AvKARE

Recalled Item: Norgestimate and Ethinyl Estradiol Tablets Recalled by AvKARE Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 2, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Sulfamethoxazole and Trimethoprim Recalled by The Harvard Drug Group LLC dba...

The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 2, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Sulfamethoxazole and Trimethoprim Recalled by The Harvard Drug Group LLC dba...

The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 2, 2025· Berkeley Advanced Biomaterials, LLC

Recalled Item: Tribio Implant 7.5mm x 40mm SB008 UDI code: Recalled by Berkeley Advanced...

The Issue: Due to incorrect product label (Incorrect product name identified on outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2025· LeMaitre Vascular, Inc.

Recalled Item: Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616 Recalled by...

The Issue: The bovine carotid arteries used to produce the impacted grafts from...

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

Class II — Potential Health HazardOngoing
DrugAugust 29, 2025· Fagron Compounding Services

Recalled Item: bevacizumab (Avastin) Injection Recalled by Fagron Compounding Services Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK System Non_DEHP Extenstion Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK System Paclitaxel Set Recalled by Baxter Healthcare Corporation...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CONTINU-FLO Solution Set Recalled by Baxter Healthcare Corporation Due to IV...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM Solution Set Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing