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. 2,476 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,476 in last 12 months

Showing 1472114740 of 27,899 recalls

Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 130 Deg 12x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Straumann Manufacturing, Inc.

Recalled Item: Neodent¿ GM Mini Conical Abutment - Product Usage: Mini Conical Recalled by...

The Issue: Laser engraved label does not match with the item in the package

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2018· Comet Technologies Usa Inc

Recalled Item: YXLON Cougar Cabinet X-Ray System Product Usage: The products are Recalled...

The Issue: Failure to meet the requirement of the performance standard for cabinet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2018· Comet Technologies Usa Inc

Recalled Item: YXLON Cheetah cabinet X-Ray System Product Usage: The products are Recalled...

The Issue: Failure to meet the requirement of the performance standard for cabinet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Countersink 1.7mm Recalled by TriMed Inc. Due to The epoxy on Apex...

The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Peg Guide Extender Recalled by TriMed Inc. Due to The spring on the...

The Issue: The spring on the PEG-Extender can rust due to the type of steel used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Locking Drill Guide Recalled by TriMed Inc. Due to The epoxy on Apex...

The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Hex Driver 1.2 Recalled by TriMed Inc. Due to The epoxy on Apex...

The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Wrist Hook Dorsal Impactor Recalled by TriMed Inc. Due to The WHD/WHV...

The Issue: The WHD/WHV impactors can rust over time due to an improper manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...

The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-900Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience has...

The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to There is a...

The Issue: There is a possibility that the liquid suction pump on some AIA-2000...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Thermal Chamber Motor Cable located in the following models:...

The Issue: Thermal chamber motors have electrical cables with single insulation rather...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Biograph mCT: a) S(64)-3R Recalled by Siemens Medical Solutions USA, Inc....

The Issue: The terminals on the plug may become loose and overheat.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Biograph Horizon a) 3R Recalled by Siemens Medical Solutions USA, Inc. Due...

The Issue: The terminals on the plug may become loose and overheat.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Aisys CS2 Anesthesia System. Sold under the following product names: AISYS...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Touchscreen display kit. Sold under the following product names: TOUCHSCREEN...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer. In vitro diagnostic testing of clinical Recalled...

The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer. In vitro diagnostic testing of clinical Recalled...

The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...

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

Class II — Potential Health HazardOngoing