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. 1,667 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
1,667 in last 12 months

Showing 4868148700 of 49,311 recalls

Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS FLEXIBLE ARTERIAL CANNULA: 8.0 MM (24 FR) 00 WITH 3/8" CONNECTOR...

The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· RAYSEARCH LABORATORIES AB

Recalled Item: Brand name: RayStation. Generic name: Treatment Planning System. Software...

The Issue: The firm decided to recall when an issue was found with the dose calculation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS HIGH-FLOW AORTIC ARCH CANNULA: 6.5 MM (20 FR) 00 WITH 3/8" CONNECTOR...

The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Covidien LP

Recalled Item: Covidien ROTICULATOR 55-4.8 Single Use Stapler REF# 017614 The RETICULA...

The Issue: Potential for the sterility barrier to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS FLEXIBLE ARTERIAL CANNULA: 6.7 MM (20 FR) 00 WITH 3/8" CONNECTOR...

The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Covidien LP

Recalled Item: Covidien ROTICULATOR 55-3.5 Single Use Stapler REF# 017612 The RETICULA...

The Issue: Potential for the sterility barrier to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CPB CATHETER KIT- DR.VAN TRIGHT. The Sarns High Flow Aortic Recalled by...

The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CUSTOM CPB CATHETER KIT-DR. The Sarns High Flow Aortic Arch Recalled by...

The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Covidien LP

Recalled Item: Covidien ROTICULATOR 30-3.5 Single Use Stapler REF# 017615 The RETICULA...

The Issue: Potential for the sterility barrier to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Covidien LP

Recalled Item: Covidien ROTICULATOR 30-4.8 Single Use Stapler REF# 017617 The RETICULA...

The Issue: Potential for the sterility barrier to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12...

The Issue: Siemens Healthcare Diagnostics has confirmed that the presence of Intrinsic...

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

Class II — Potential Health HazardOngoing
FoodMay 8, 2012· Panera Bread LLC

Recalled Item: Panera Recalled by Panera Bread LLC Due to Product ingredient statement...

The Issue: Product ingredient statement reversed for Reduced Fat Honey Walnut Cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 8, 2012· Panera Bread LLC

Recalled Item: Panera HONEY WALNUT CREAM CHEESE SPREAD Recalled by Panera Bread LLC Due to...

The Issue: Product ingredient statement reversed for Reduced Fat Honey Walnut Cream...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 8, 2012· Morton Salt Co.

Recalled Item: Morton Recalled by Morton Salt Co. Due to Impurities/Degradation Products:...

The Issue: Impurities/Degradation Products: The product was found to contain a slightly...

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

Class III — Low RiskOngoing
Refund
DrugMay 8, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Recalled by Hill...

The Issue: Subpotent; fluocinolone acetonide

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

Class III — Low RiskOngoing
Refund
DrugMay 8, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Topical Oil (Scalp Oil)...

The Issue: Subpotent; fluocinolone acetonide

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

Class III — Low RiskOngoing
Refund
FoodMay 8, 2012· Seoul Shik Poom, Inc.

Recalled Item: Frozen Salted Clam Recalled by Seoul Shik Poom, Inc. Due to Korean Certified...

The Issue: Korean Certified Shippers delisted from ICSSL.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 8, 2012· Seoul Shik Poom, Inc.

Recalled Item: Frozen Oysters Recalled by Seoul Shik Poom, Inc. Due to Korean Certified...

The Issue: Korean Certified Shippers delisted from ICSSL.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 7, 2012· Non-Invasive Monitoring Systems, Inc.

Recalled Item: USA-002 Rev A brochure is a two sided tri-fold printed Recalled by...

The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· JK Products & Services, Inc

Recalled Item: BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human...

The Issue: The Beauty Angel was marketed without a 510k.

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

Class II — Potential Health HazardOngoing