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. 2,579 recalls have been distributed to New Hampshire in the last 12 months.
Showing 2221–2240 of 49,311 recalls
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories, LLC Due to...
The Issue: Failed Impurities/Degradation Specifications An out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spectrum Advanced Gel Hand Sanitizer Recalled by Consumer Product Partners,...
The Issue: Subpotent product: Product has cloudy appearance and tested below assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to GE HealthCare...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA PET/MR Recalled by GE Medical Systems, LLC Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w 3.0T Recalled by GE Medical Systems, LLC Due to GE...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apex Knee System. Model Numbers: KC-50090 Recalled by CORIN MEDICAL, LTD....
The Issue: Investigation has identified that the age of the nylon packaging material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroMyst Applicator Recalled by Integra LifeSciences Corp. (NeuroSciences)...
The Issue: Lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is...
The Issue: Due to a software bug the robotic arm may incorrectly guide the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetaminophen Tablets Recalled by Aurobindo Pharma USA Inc Due to cGMP...
The Issue: cGMP deviations: Due to confirmed consumer complaints received with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IontoPatch 80 Recalled by LTS Therapy Systems, LLC Due to The nonwoven pads...
The Issue: The nonwoven pads in the device do not absorb the saline solution or any...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IontoPatch STAT Recalled by LTS Therapy Systems, LLC Due to The nonwoven...
The Issue: The nonwoven pads in the device do not absorb the saline solution or any...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemodynamics Software Recalled by CHANGE...
The Issue: Due to complaints, software update may cause software to unexpectedly shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemo Software Recalled by CHANGE HEALTHCARE...
The Issue: Due to complaints, software update may cause software to unexpectedly shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....
The Issue: Devices contain potentially out-of-specification levels of endotoxins and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....
The Issue: Devices contain potentially out-of-specification levels of endotoxins and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog...
The Issue: The Instructions for Use do not match the 510(k) FDA cleared indications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.