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. 2,508 recalls have been distributed to New Hampshire in the last 12 months.
Showing 12081–12100 of 27,899 recalls
Recalled Item: Getinge 88-Series-washer disinfectors intended for cleaning Recalled by...
The Issue: Potential leakage that may occur due to ruptured spot welds in the chamber,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kits containing Covidien Force TriVerse Electrosurgical Devices. Distributed...
The Issue: Sterile packaging may potentially be compromised, and use of products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Force TriVerse Electrosurgical Devices Recalled by Covidien Llc Due...
The Issue: Sterile packaging may potentially be compromised, and use of products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuraGen Nerve Guide Recalled by Integra LifeSciences Corp. Due to...
The Issue: Nonconforming product which was dispositioned for rejection was mistakenly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys CA 19-9 Recalled by Roche Diagnostics Operations, Inc. Due to The...
The Issue: The firm has received an increased number of complaints concerning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems E2 Estradiol Catalog #: US: L2KE22(D) (200 Recalled by...
The Issue: Due to high discordant Estradiol results which.potentially affects all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and Recalled by...
The Issue: Due to high discordant Estradiol results which.potentially affects all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMO-7 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....
The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMO-10 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....
The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris System Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris PCA Module Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris Pump Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX PLUS Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal PS Knee Replacement System Recalled by Conformis, Inc. Due to A...
The Issue: A limited number of tibial trays were labeled with an incorrect serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Knee Replacement System Recalled by Conformis, Inc. Due to A...
The Issue: A limited number of tibial trays were labeled with an incorrect serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (3/4 Force). REF/UDI::A1603/(01)00607915110581...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/4 Force). REF/UDI::A1602/(01)00607915110574...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.