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.
Showing 6681–6700 of 27,899 recalls
Recalled Item: Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable...
The Issue: There have been complaints that the clip did not come out of the tube sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro Patient Monitor is a portable vital signs monitor Recalled by...
The Issue: During internal testing, Regulatory Compliance issues were identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...
The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...
The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...
The Issue: Incorrect labeling; specifically, the product name, lot number and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...
The Issue: Incorrect labeling; specifically, the product name, lot number and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Lysis Beads Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent GM X 6mm Engaging Titanium Base Recalled by Preat Corp Due to...
The Issue: Engaging titanium base contains a dimensional condition that allows vertical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD with RVD Enhancer: a) 1 mL Recalled by Entopsis , Inc....
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis BCSNano (1mL) Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Support: a) 1 mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD-RT Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Activator: a) 1.5mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent Buccal Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPerfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2D Perfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to There...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a...
The Issue: Battery leakage can cause corrosion to the metal enclosure near the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agilent Resolution ctDx FIRST Sample Collection Kit Recalled by AGILENT...
The Issue: Distributed sample collection kit with an unapproved instruction for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raystation treatment planning system for radiation therapy Recalled by...
The Issue: It is possible to set a non-zero collimator angle in the Virtual Simulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.