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. 2,563 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,563 in last 12 months

Showing 34413460 of 27,899 recalls

Medical DeviceJuly 18, 2024· Centinel Spine, Inc.

Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...

The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2024· Becton Dickinson & Co.

Recalled Item: BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for Recalled by...

The Issue: May intermittently produce falsely resistant results for pyrazinamide (PZA)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2024· Centinel Spine, Inc.

Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...

The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Mazor Robotics Ltd

Recalled Item: Mazor X. Model Number Recalled by Mazor Robotics Ltd Due to Software...

The Issue: Software anomalies which can result in two separate issues: A lagging screen...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Boston Scientific Neuromodulation Corporation

Recalled Item: WAVEWRITER ALPHA: Model: SC-1216 Recalled by Boston Scientific...

The Issue: Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter...

The Issue: The Spectrum WBM may fail to auto-document infusion status information back...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Beckman Coulter Biomedical GmbH

Recalled Item: PE Centrifuge Temperature Controlled Recalled by Beckman Coulter Biomedical...

The Issue: The adhesive joint between the plastic socket and metal component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Beckman Coulter Biomedical GmbH

Recalled Item: PE Centrifuge Recalled by Beckman Coulter Biomedical GmbH Due to The...

The Issue: The adhesive joint between the plastic socket and metal component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Beckman Coulter Biomedical GmbH

Recalled Item: Power Express Recalled by Beckman Coulter Biomedical GmbH Due to The...

The Issue: The adhesive joint between the plastic socket and metal component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Baxter Healthcare Corporation

Recalled Item: Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter Healthcare...

The Issue: The Spectrum WBM may fail to auto-document infusion status information back...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Firm has released a...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SATINSLIT FULL HANDLE3.0MM ANG...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ TOTALPLUSr CP PAK 20K CPM BWV .9 Recalled by Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ CMB PAK 10K CPM Recalled by Alcon Research LLC Due to...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: ClearCut Sideport Knife Dual Bevel 1.2mm...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ TOTALPLUS CP PAK 20K CPM BV .9 Recalled by Alcon Research...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: TOTAL PLUS Recalled by Alcon Research LLC Due to Alcon has...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ CMB PAK 7.5CPM Recalled by Alcon Research LLC Due to Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing