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. 1,102 recalls have been distributed to New Hampshire in the last 12 months.
Showing 1901–1920 of 49,311 recalls
Recalled Item: H-E-B Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Subpotent Drug-...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RITE AID PHARMACY Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ReliOn Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Subpotent...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Good Neighbor Pharmacy Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent...
The Issue: Certain batches are being removed due to an increase in complaints received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective Container: spike of the cap becomes lodged in the nozzle of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: C5-2 Lumify Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3D6-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S9-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C8-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X6-1 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNI II TEE Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C9-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSDUCER L12-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C8-4v Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L9-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eL18-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.