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. 2,409 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,409 in last 12 months

Showing 2064120660 of 27,899 recalls

Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548320 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549530 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549470 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-450XT5 Operation Manual: Cleaning Recalled by Fujifilm Medical...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope Recalled by Fujifilm Medical Systems U.S.A., Inc. Due to This...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-250XT5 Operations Manual: Cleaning Disinfection and Storage...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548660 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-450XL5 Operation Manual: Cleaning Recalled by Fujifilm Medical...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-250XL5 Operations Manual: Cleaning Recalled by Fujifilm Medical...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548450 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· MOOG Medical Devices Group

Recalled Item: Moog Curlin Infusion Recalled by MOOG Medical Devices Group Due to Moog is...

The Issue: Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Cardinal Scale Mfg Co

Recalled Item: Cardinal Recalled by Cardinal Scale Mfg Co Due to One complaint of a seat on...

The Issue: One complaint of a seat on a scale failing unexpectedly which can cause an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548340 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Plaza Picture archiving and communication system. Software only. PACS...

The Issue: Siemens is releasing an updated software version to address several software...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: STD KIT GK213 Recalled by Applied Medical Resources Corp Due to Applied...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Hospira Inc.

Recalled Item: The Symbiq infusion pump is a device used in a Recalled by Hospira Inc. Due...

The Issue: Potential for the Symbiq pole clamp assemblies to be missing the rubber stop...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: STD GK258 Recalled by Applied Medical Resources Corp Due to Applied Medical...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Bio-Rad Laboratories, Inc.

Recalled Item: EVOLIS Microplate System Recalled by Bio-Rad Laboratories, Inc. Due to The...

The Issue: The error "Washer Reagent Clean Fluid" level low alarmed, which prompted the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: STD KIT GK260 Recalled by Applied Medical Resources Corp Due to Applied...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Draeger Medical, Inc.

Recalled Item: Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number:...

The Issue: Drager became aware of situations where the error message "Poti unplugged"...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing