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.

49,311 total recalls
2,558 in last 12 months

Showing 53215340 of 49,311 recalls

DrugMay 28, 2024· Organon Llc

Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container

The Issue: Defective Container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 28, 2024· Sagent Pharmaceuticals

Recalled Item: Docetaxel Injection Recalled by Sagent Pharmaceuticals Due to Presence of...

The Issue: Presence of Particulate Matter: Presence of particulate matter from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 28, 2024· Organon Llc

Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container

The Issue: Defective Container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 28, 2024· Organon Llc

Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container

The Issue: Defective Container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMay 28, 2024· Artivion, Inc

Recalled Item: (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch Recalled...

The Issue: Grafts were found to have been approved, released, shipped and implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2024· Artivion, Inc

Recalled Item: CryoValve SG Pulmonary Human Heart Valve Recalled by Artivion, Inc Due to...

The Issue: Grafts were found to have been approved, released, shipped and implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-FR Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-V Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-CR Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to LIH Influence check...

The Issue: LIH Influence check settings for Lipemia are incorrect which may result...

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

Class II — Potential Health HazardOngoing
DrugMay 24, 2024· SYNCHRONICITY SPA INC, DBA SUNTE

Recalled Item: suntegrity Recalled by SYNCHRONICITY SPA INC, DBA SUNTE Due to CGMP Deviations

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2024· SYNCHRONICITY SPA INC, DBA SUNTE

Recalled Item: suntegrity Recalled by SYNCHRONICITY SPA INC, DBA SUNTE Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: Presence of Aspergillus...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 24, 2024· CUE HEALTH INC

Recalled Item: Cue Health COVID-19 Test Cartridge Cue COVID-19 Test Recalled by CUE HEALTH...

The Issue: Due to modified test kits being marketed and distributed without FDA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2024· WOM World Of Medicine AG

Recalled Item: WOM Tube Set for lrrlgatlon Recalled by WOM World Of Medicine AG Due to...

The Issue: Incorrect transponder data was written on the RFID tags triggers the error...

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

Class II — Potential Health HazardOngoing
DrugMay 23, 2024· Eugia US LLC

Recalled Item: Dexamethasone Sodium Phosphate injection USP Recalled by Eugia US LLC Due to...

The Issue: Failed Impurities/Degradation Specifications: impurity sulfonic acid adduct...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zoledronic Acid Injection 5mg/100mL Sterile Solution Recalled by Dr. Reddy's...

The Issue: Lack of Assurance of Sterility: Leaking vials

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 23, 2024· Alcon Research LLC

Recalled Item: Surgical Image Guidance Functionality Recalled by Alcon Research LLC Due to...

The Issue: After surgery initiation, while using surgical image guidance, if...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2024· Howmedica Osteonics Corp.

Recalled Item: Gray Revision Instrument System Accessory Tray/Case Recalled by Howmedica...

The Issue: The design of the HRIS Storage & Sterilization Case and Tray P/N 6210-9-900...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2024· Howmedica Osteonics Corp.

Recalled Item: HRIS Storage & Sterilization Case and Tray Recalled by Howmedica Osteonics...

The Issue: The design of the HRIS Storage & Sterilization Case and Tray P/N 6210-9-900...

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

Class II — Potential Health HazardOngoing
DrugMay 22, 2024· MexHealth LLC

Recalled Item: OSSOS-SANS con: Glucosamina Curcuma Ortiga tablets Recalled by MexHealth LLC...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund