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. 1,039 recalls have been distributed to New Hampshire in the last 12 months.
Showing 15761–15780 of 49,311 recalls
Recalled Item: Remel Haemophilus Test Medium (150 mm) 10/PK Recalled by Remel Inc Due to...
The Issue: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio X.pree Recalled by Siemens Medical Solutions USA, Inc Due to A patient...
The Issue: A patient image was assigned to a different patient during image recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Haemophilus Test Medium(100mm) 10/PK Recalled by Remel Inc Due to When...
The Issue: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics SafeSheath ULTRALITE 10F Recalled by Oscor, Inc. Due to...
The Issue: Potential for open seal on sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A610 Clinician Programmer Application for Deep Brain Stimulation Clinician...
The Issue: There are two issues within this correction action: 1. Cycling Issue: When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% SODIUM CHLORIDE Irrigation Recalled by ICU Medical Inc Due to Presence...
The Issue: Presence of particulate matter.one confirmed customer report of particulate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Oral Solution Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIOTRONIK INTICA NEO 7 HF-T DF-1 IS-1 ProMRI Recalled by BIOTRONIK Inc Due...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow OnControl Bone Lesion Biopsy System Tray-11 ga 10 cm Recalled by Arrow...
The Issue: Difficulty inserting the biopsy ejector rod into the bone lesion biopsy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK IPERIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK INTICA NEO 7 VR-T DX DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA NEO 7 VR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Iperia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Iforia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Iforia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.