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. 1,019 recalls have been distributed to New Hampshire in the last 12 months.
Showing 16501–16520 of 49,311 recalls
Recalled Item: Revolution CT with Apex Edition CT System - Product Usage: intended for head...
The Issue: A potential for protocol(s) with unintended patient orientation or scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Gamma-Glutamyl Transferase (GGT) Reagent - Product Usage: For in...
The Issue: Gamma-Glutamyl Transferase (GGT) Reagent Low End Repeatability-Imprecision....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...
The Issue: There is the potential for the compounding system to not immediately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...
The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIAISON 1-84 PTH Assay - Product Usage: is an in Recalled by Diasorin Inc....
The Issue: Potential for system to produce falsely elevated parathyroid hormone (PTH)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...
The Issue: There is the potential for the compounding system to not immediately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...
The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien TA Auto Suture Vascular Loading Unit with DST Series Recalled by...
The Issue: May contain a damaged internal component which could impede staple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...
The Issue: Failed Impurity/Degradation Specifications: Unidentified impurities not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Scandonest 3% Plain (Mepivacaine Hydrochloride 3% without Vasoconstrictor)...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 11 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 1 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 5 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 6 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Automation Solutions Recalled by Ortho-Clinical Diagnostics, Inc. Due...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced Recalled by Maquet Cardiovascular Us Sales, Llc Due to The...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Rod Cutter Recalled by Zimmer Biomet, Inc. Due to Device has the...
The Issue: Device has the potential for fracture during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.