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. 2,545 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,545 in last 12 months

Showing 68016820 of 27,899 recalls

Medical DeviceJanuary 30, 2023· DiaSorin Molecular LLC

Recalled Item: Simplexa Flu A/B & RSV Direct Gen II Recalled by DiaSorin Molecular LLC Due...

The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Carestream Health, Inc.

Recalled Item: DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For...

The Issue: After pressing and releasing the Z-Axis Motorized buttons on the Tube Head...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Triglycerides (concentrated)-In vitro diagnostic use in the...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH LDL Cholesterol Direct (DLDL)-In vitro diagnostic quantitative...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Total Protein II- In vitro diagnostic use in Recalled by Siemens...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Triglycerides_2: in vitro diagnostic use in the quantitative...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2023· Beckman Coulter, Inc.

Recalled Item: Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N)...

The Issue: An increased incidence of damage to the nut band from a new vendor (Boamax)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2023· CooperVision, Inc.

Recalled Item: Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)...

The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2023· CooperVision, Inc.

Recalled Item: Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens...

The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Church & Dwight Inc

Recalled Item: Easy Read App associated with First Response Pregnancy Test Sticks Recalled...

The Issue: Church & Dwight First Response Pregnancy Kits was marketed with the Easy...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Covidien, LP

Recalled Item: Tri-Staple 2.0 Black Intelligent Reload Recalled by Covidien, LP Due to...

The Issue: Affected lots have the potential for a broken sled vane, which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Stryker Corporation

Recalled Item: Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the...

The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Baxter Healthcare Corporation

Recalled Item: Life2000 Ventilator PKG Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is the potential for patient desaturation events to occur under...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 25, 2023· Stryker Corporation

Recalled Item: Finished Goods Box of 50 Inserts and Scanning Labels for Recalled by Stryker...

The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Baxter Healthcare Corporation

Recalled Item: Life2000 Ventilator PKG Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is the potential for patient desaturation events to occur under...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 25, 2023· Baxter Healthcare Corporation

Recalled Item: Life2000 Ventilator System Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is the potential for patient desaturation events to occur under...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 25, 2023· Stryker Corporation

Recalled Item: Finished Goods Box of 50 Inserts and Scanning Labels for Recalled by Stryker...

The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Baxter Healthcare Corporation

Recalled Item: Life2000 Ventilator Recalled by Baxter Healthcare Corporation Due to There...

The Issue: There is the potential for patient desaturation events to occur under...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 24, 2023· Outset Medical, Inc.

Recalled Item: Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a Recalled...

The Issue: An observed trend of high conductivity dialysate alarms in a hemodialysis...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2023· Intuitive Surgical, Inc.

Recalled Item: Patient Side Cart Recalled by Intuitive Surgical, Inc. Due to Preventative...

The Issue: Preventative maintenance data was used to identify instrument Arms, part of...

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

Class II — Potential Health HazardOngoing