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. 2,540 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,540 in last 12 months

Showing 92619280 of 13,374 recalls

DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Novolin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Ascorbic Acid 500 MG/ML Inj. Recalled by RemedyRepack Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Vitamin B-Complex 100 Recalled by RemedyRepack Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Bicillin L-A 600000 Units/mL Inj. Recalled by RemedyRepack Inc. Due to...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2015· Northwind Pharmaceuticals LLC

Recalled Item: Prednisone 20 mg Recalled by Northwind Pharmaceuticals LLC Due to Labeling:...

The Issue: Labeling: Not elsewhere classified. NDC number is incorrect on the container.

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

Class III — Low RiskOngoing
Refund
DrugNovember 9, 2015· Freedom Pharmaceuticals Inc

Recalled Item: Baclofen USP powder Recalled by Freedom Pharmaceuticals Inc Due to Presence...

The Issue: Presence of Foreign Substance

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 2.5 mg/0.1 mL in 3/10 mL 31 G 5/16" Recalled by Pine...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 2 mg/0.08 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 1.25 mg/0.05 mL filled to 0.06 mL in 3/10 Recalled by Pine...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 1.25 mg/0.05 mL in 3/10 mL 31 G 5/16" Recalled by Pine...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...

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

Class III — Low RiskOngoing
Refund
DrugNovember 2, 2015· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Meclizine Hydrochloride Tablets Recalled by Mylan Institutional, Inc....

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 29, 2015· Amerisource Health Services

Recalled Item: HYDROCHLOROTHIAZIDE CAPSULES Recalled by Amerisource Health Services Due to...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2015· Sanofi-Aventis U.S. LLC

Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: Defective Delivery System; potential to have inaccurate dosage delivery

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 28, 2015· Sanofi-Aventis U.S. LLC

Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: Defective Delivery System; potential to have inaccurate dosage delivery

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 27, 2015· Geritrex Corp

Recalled Item: Carbo-O-Philic 40 Cream 40% (Urea) tubes Recalled by Geritrex Corp Due to...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 27, 2015· Geritrex Corp

Recalled Item: GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories Recalled by...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 27, 2015· Geritrex Corp

Recalled Item: Carbo-O-Philic 40 Gel 40% (Urea) NET WT tube Recalled by Geritrex Corp Due...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund