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. 2,540 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,540 in last 12 months

Showing 78417860 of 27,899 recalls

Medical DeviceJune 14, 2022· GE Healthcare, LLC

Recalled Item: Centricity PACS Software Version 7.0 SP0.0.4.7 Recalled by GE Healthcare,...

The Issue: The Event Notification Manager (ENM) functionality for certain products does...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2022· SIGHT DIAGNOSTICS LTD

Recalled Item: Sight OLO Recalled by SIGHT DIAGNOSTICS LTD Due to The default ranges for...

The Issue: The default ranges for MCH, MCHC, and RDW for age group "Child 2-11y" are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2022· R & D Systems, Inc.

Recalled Item: Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative...

The Issue: The Instructions for Use (IFU, Part Number 750095) provided with the...

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

Class III — Low RiskOngoing
Medical DeviceJune 14, 2022· Wright Medical Technology, Inc.

Recalled Item: Wright EVOLVE TRIAD Plate Cutter Recalled by Wright Medical Technology, Inc....

The Issue: The plate cutter is unable to meet sterilization requirements when it is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2022· Guangdong Haiou Medical Apparatus Co., Ltd

Recalled Item: Haiou Needle Retractable Safety Syringe with Needle-1ML 23G x 1 Recalled by...

The Issue: Complaints received in which needle and needle holder have detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2022· Guangdong Haiou Medical Apparatus Co., Ltd

Recalled Item: HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G...

The Issue: Complaints received in which needle and needle holder have detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Pheno Recalled by Siemens Medical Solutions USA, Inc Due to A video...

The Issue: A video signal from one of the transceivers of the Large Display may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2022· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 11B Recalled by RAYSEARCH LABORATORIES AB Due to This notice...

The Issue: This notice concerns two issues found related to the display of Linear...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Randox Laboratories Ltd.

Recalled Item: Soluble Transferrin Receptors (STFR) Recalled by Randox Laboratories Ltd....

The Issue: A customer reported a problem with the reagent and calibrator. Randox...

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

Class III — Low RiskOngoing
Medical DeviceJune 9, 2022· Randox Laboratories Ltd.

Recalled Item: Soluble Transferrin Receptors Calibrator Series (STFR CAL) Recalled by...

The Issue: A customer reported a problem with the reagent and calibrator. Randox...

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

Class III — Low RiskOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolMax ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolFit ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCurve ZELTIQ Vaccum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCurve+ ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCore ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott

Recalled Item: Abbott TactiCath Sensor Enabled Recalled by Abbott Due to When connected to...

The Issue: When connected to the EnSite Precision Navigation System, an affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome HSI Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision Chronic Catheter Recalled by Covidien Llc Due to There...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision HSI Chronic Catheter Recalled by Covidien Llc Due to...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome H Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing