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. 2,466 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,466 in last 12 months

Showing 1614116160 of 27,899 recalls

Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK TU Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK HGH Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK AFP Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK C-Peptide Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK hsE2 Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh ST AIA-PACK HbA1c Control Recalled by Tosoh Bioscience Inc Due to The...

The Issue: The assay can potentially generate erroneously elevated or erroneously...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh ST AIA-PACK HbA1c Calibrator Recalled by Tosoh Bioscience Inc Due to...

The Issue: The assay can potentially generate erroneously elevated or erroneously...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Testosterone Recalled by Tosoh Bioscience Inc Due to Asfotase...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Cort Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Prolactin Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Getinge Disinfection Ab

Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...

The Issue: There is potential for a cart with disinfected goods to unload without the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Randox Laboratories Ltd.

Recalled Item: Lipase Recalled by Randox Laboratories Ltd. Due to Randox has now released...

The Issue: Randox has now released further steps to avoid contamination of the Lipase...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Beckman Coulter Inc.

Recalled Item: BECKMAN COULTER iChemVELOCITY Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has determined that there is a potential for incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Getinge Disinfection Ab

Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...

The Issue: There is potential for a cart with disinfected goods to unload without the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius Tiro Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Premium Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius Tiro M Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius MRI Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· bioMerieux, Inc.

Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to Several complaints were...

The Issue: Several complaints were received for invalid calibration with low calibrator...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Insertion Tray Recalled by Vygon U.S.A. Due to Potential...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing