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 4030140320 of 49,311 recalls

Medical DeviceOctober 6, 2014· Beckman Coulter Inc.

Recalled Item: UniCel DxC 600i SYNCHRON Access Clinical Analyzer Recalled by Beckman...

The Issue: Beckman Coulter is recalling the Small Form Factor Console PC (SFF PC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Elekta, Inc.

Recalled Item: Laksell Gamma Knife Perfexion Recalled by Elekta, Inc. Due to Elekta has...

The Issue: Elekta has become aware that the latches may be locked before they have been...

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

Class II — Potential Health HazardOngoing
DrugOctober 3, 2014· Wisconsin Pharmacal Company

Recalled Item: CVS pharmacy Recalled by Wisconsin Pharmacal Company Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: CVS Pharmacy Pain Relieving...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2014· Sagent Pharmaceuticals Inc

Recalled Item: Ketorolac Tromethamine INJECTION Recalled by Sagent Pharmaceuticals Inc Due...

The Issue: Incorrect or Missing Lot and/or Exp Date: Ketorolac Tromethamine Injection,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips IntelliVue Monitors with software revisions J.21.03 Recalled by...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips Avalon Monitors with software revision J.30.58: Model Product FM20...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
DrugOctober 2, 2014· Sandoz, Inc

Recalled Item: candesartan cilexetil Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: An Out of Specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2014· Valeant Pharmaceuticals International

Recalled Item: Locoid (hydrocortisone butyrate 0.1%) Recalled by Valeant Pharmaceuticals...

The Issue: Subpotent Drug; for the active, HCB, and preservatives, Propylparaben and...

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2014· Valeant Pharmaceuticals International

Recalled Item: Hydrocortisone Butyrate Cream 0.1% Recalled by Valeant Pharmaceuticals...

The Issue: Subpotent Drug; for the active, HCB, and preservatives, Propylparaben and...

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

Class III — Low RiskOngoing
Refund
FoodOctober 2, 2014· Family Dollar Stores - NC Distribution Center

Recalled Item: Family Gourmet Long Grain Enriched White Rice in 32 oz. Recalled by Family...

The Issue: Possible insect infestation

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 2, 2014· Zimmer, Inc.

Recalled Item: Natural Knee II Revision Femoral Stem Recalled by Zimmer, Inc. Due to Failed...

The Issue: Failed to meet established requirements for sterile barrier integrity due to...

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

Class II — Potential Health HazardOngoing
DrugOctober 1, 2014· Zydus Pharmaceuticals USA Inc

Recalled Item: Amlodipine Besylate Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Discoloration: Brown spots were noted embedded in Amlodipine Besylate...

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2014· Hospira Inc.

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by Hospira Inc. Due to Lack...

The Issue: Lack Of Assurance Of Sterility: Confirmed customer complaints of glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2014· Avella of Deer Valley, Inc.

Recalled Item: HYDROXYPROGESTERONE CAPROATE 250 MG/ML (IN SESAME OIL) Recalled by Avella of...

The Issue: Crystallization: Formation of crystals observed in product.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 1, 2014· Markpol Distributors Inc.

Recalled Item: Kupiec Rice Cakes with Dark Chocolate Recalled by Markpol Distributors Inc....

The Issue: This voluntary recall has been initiated because the Kupiec Rice Cakes with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 1, 2014· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Covidien Puritan Bennett 980 Ventilator Recalled by Nellcor Puritan Bennett...

The Issue: Covidien is recalling certain Puritan Bennett 980 Ventilator Systems due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 1, 2014· Roscoe Medical Inc

Recalled Item: Transport Rollator with Padded Seat Recalled by Roscoe Medical Inc Due to...

The Issue: The caster may separate completely from the device frame causing injury to user.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer Dental Inc

Recalled Item: Tapered Screw-Vent Implant Recalled by Zimmer Dental Inc Due to Zimmer...

The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Medartis, Inc.

Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...

The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer Dental Inc

Recalled Item: Spline Twist Implant Recalled by Zimmer Dental Inc Due to Zimmer Dental is...

The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...

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

Class II — Potential Health HazardOngoing