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. 2,558 recalls have been distributed to New Hampshire in the last 12 months.
Showing 4761–4780 of 27,899 recalls
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023 Recalled by Brasseler...
The Issue: The device has a grip detail (right angle latch) out of specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.2.100 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.1.000 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.2.000 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.1.000US Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.3.000 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.2.200 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.