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.
Showing 7181–7200 of 49,311 recalls
Recalled Item: Lubricant Gel Drops (Polyethylene glycol 400 0.4% Recalled by Kilitch...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lubricant Gel Drops (Carboxymethylcellulose sodium 1.0%) Recalled by Kilitch...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader brand Dry Eye Relief (Polyethylene glycol 400 0.4% and Recalled by...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lubricant Eye Drops (Propylene glycol 0.6%) Recalled by Kilitch Healthcare...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KinderMed INFANTS' PAIN & FEVER Acetaminophen Recalled by KINDER FARMS LLC...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KinderMed KIDS' PAIN & FEVER Acetaminophen Recalled by KINDER FARMS LLC Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calibration Serum Level 3. CAL 3 Recalled by Randox Laboratories Ltd. Due to...
The Issue: There have been transcription errors on the Instructions For Use (IFU) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORI REAL INTELLIGENCE Robotic Drill Recalled by Blue Belt Technologies, Inc...
The Issue: Possibility that the user is unable to resolve drill disconnection error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS...
The Issue: Identification label on affected hookups could become illegible over time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous probe connection cable ( and 701048804) used with Recalled by Maquet...
The Issue: Firm received complaints of breaks in the insulation, shielding, or wires of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide 1% (10mg/mL) Recalled by Fagron Compounding Services Due to...
The Issue: Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Gel Recalled by Teva Pharmaceuticals USA, Inc Due to OOS for...
The Issue: OOS for viscosity
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 6-7-8. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.