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 34413460 of 49,311 recalls

Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Recalled...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) MTO Recalled by MEDLINE...

The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) FDS Recalled by MEDLINE...

The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 16, 2024· Olympus Corporation of the Americas

Recalled Item: LithoCrushV Single Use Mechanical Lithotriptor V. Model Number:...

The Issue: Potential for distal tip tearing of the Mechanical Lithotriptor V.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2024· Alphatec Spine, Inc.

Recalled Item: Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1)...

The Issue: Complaints have been received regarding post-operative implant collapse.

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

Class II — Potential Health HazardOngoing
FoodDecember 13, 2024· MR BING FOODS INC.

Recalled Item: Mr. Bing brand Sriracha Chili Sauce Recalled by MR BING FOODS INC. Due to...

The Issue: Product may contain spoilage organisms.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 13, 2024· Amerisource Health Services LLC

Recalled Item: Clobazam Tablets Recalled by Amerisource Health Services LLC 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
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Wolf-Pak Product Name: Premium Dressing Change Kit with Recalled...

The Issue: Potential for hole in package compromising sterility of the medical kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: IMed Products Product Name: Dressing Change Kit with Recalled by...

The Issue: Potential for hole in package compromising sterility of the medical kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Cloth Recalled...

The Issue: Potential for hole in package compromising sterility of the medical kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Transparent...

The Issue: Potential for hole in package compromising sterility of the medical kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Tacy Medical Recalled by Trinity Sterile, Inc. Due to Potential...

The Issue: Potential for hole in package compromising sterility of the medical kit.

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

Class II — Potential Health HazardOngoing
DrugDecember 12, 2024· Akron Pharma, Inc.

Recalled Item: Acetaminophen Recalled by Akron Pharma, Inc. Due to Labeling: Not Elsewhere...

The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2024· Akron Pharma, Inc.

Recalled Item: Diphenhydramine HCl 25 mg Recalled by Akron Pharma, Inc. Due to Labeling:...

The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2024· Akron Pharma, Inc.

Recalled Item: Diphenhydramine HCl 50 mg Recalled by Akron Pharma, Inc. Due to Labeling:...

The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2024· Akron Pharma, Inc.

Recalled Item: Acetaminophen Regular Strength Recalled by Akron Pharma, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2024· Akron Pharma, Inc.

Recalled Item: Diphenhydramine HCl 25 mg Recalled by Akron Pharma, Inc. Due to Labeling:...

The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2024· Akron Pharma, Inc.

Recalled Item: Acetaminophen Extra Strength 500 mg Recalled by Akron Pharma, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

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

Class III — Low RiskOngoing
Refund