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. 956 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
956 in last 12 months

Showing 37381–37400 of 49,311 recalls

DrugMay 18, 2015· Advanced Physician Solutions, Inc.

Recalled Item: GLUTATHIONE 200MG/ML (STERILE WATER) (30ML Recalled by Advanced Physician...

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
DrugMay 18, 2015· Advanced Physician Solutions, Inc.

Recalled Item: DMSO (STERILE WATER) SOLUTION -50ML VIAL 50% INJECTABLE Recalled by Advanced...

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
DrugMay 18, 2015· Advanced Physician Solutions, Inc.

Recalled Item: NANPYRIDOXINE (STERILE WATER) 30ML 50MG/ML INJECTABLE Recalled by Advanced...

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
DrugMay 18, 2015· Advanced Physician Solutions, Inc.

Recalled Item: ESTRADIOL VALERATE (SESAME OIL) 10ML VIAL 10MG/ML INJECTABLE Recalled by...

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 DeviceMay 15, 2015· MedtestDx, Inc.

Recalled Item: MedTest DX Control Reconstitution Fluid Kit configuration: 20 x 5 Recalled...

The Issue: Vial to vial variation in the fill volume that could affect control recovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via and Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: measurements drawn on the 2nd and subsequent images of the series are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· Philips Ultrasound, Inc.

Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound, Inc. Due to Philips...

The Issue: Philips Healthcare has discovered a problem in the Philips Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· ArthroCare Medical Corporation

Recalled Item: EVAC 70 XTRA with Integrated Cable Product Usage: Recalled by ArthroCare...

The Issue: Potential component failure causing device inoperability

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· ArthroCare Medical Corporation

Recalled Item: PROcise XP Wand with Integrated Cable Product Usage: Recalled by ArthroCare...

The Issue: Potential component failure resulting in inoperability

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· Veridex, LLC

Recalled Item: Cell Search Circulating Tumor Kit. Intended for the enumeration of Recalled...

The Issue: Complaints of the presence of artifacts that appears as small bead like...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2015· Teleflex Medical

Recalled Item: Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson...

The Issue: The intake port may be blocked which can cause the bag to fail to fill.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2015· Cook Inc.

Recalled Item: LapSac Surgical Tissue Pouch. The current intended use for the Recalled by...

The Issue: Includes Information not stated in the intended use.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2015· BIOMET FRANCE S.A.R.L.

Recalled Item: The Optigun Ratchet is a hand-held cement gun for use Recalled by BIOMET...

The Issue: The pin which maintains the knob button, may disconnect and become lost....

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

Class II — Potential Health HazardOngoing
FoodMay 14, 2015· Aurora Products, Inc.

Recalled Item: Raw Macadamia Nuts Recalled by Aurora Products, Inc. Due to Potential...

The Issue: Product contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 13, 2015· Mondelez International

Recalled Item: Outer carton : Nabisco Newtons Fig 24-2 OZ (56 g) Recalled by Mondelez...

The Issue: Fig Newtons brand Club Super Carton cookie products is mislabeled. The outer...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 13, 2015· The Binding Site Group, Ltd.

Recalled Item: Optilite Analyser Recalled by The Binding Site Group, Ltd. Due to Potential...

The Issue: Potential risk of the Optilite lid/cover falling suddenly and causing injury...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2015· Ethicon Endo-Surgery Inc

Recalled Item: SEDASYS Computer-Assisted Personalized Sedation System Recalled by Ethicon...

The Issue: Ethicon has found that disinfecting methods not specified in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 13, 2015· Synthes, Inc.

Recalled Item: 3.2 mm Cannulated Drill Bit/ QC 170 mm 2.7 Cannulated Recalled by Synthes,...

The Issue: affected parts and lots of the Cannulated Drill Bits have the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2015· Bio-Rad Laboratories, Inc.

Recalled Item: The spare component Anti-HBs Cutoff Calibrator Recalled by Bio-Rad...

The Issue: The spare component Anti-HBs Cutoff Calibrator, Catalog number 26154, is...

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

Class III — Low RiskOngoing
Medical DeviceMay 13, 2015· Synthes, Inc.

Recalled Item: 3.7mm Cannulated Locking Screws and 3.7mm Cannulated Conical Screws Recalled...

The Issue: Certain lots of the 3.7mm Cannulated Locking Screws and 3.7mm Cannulated...

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

Class II — Potential Health HazardOngoing