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. 2,409 recalls have been distributed to New Hampshire in the last 12 months.
Showing 18901–18920 of 27,899 recalls
Recalled Item: Alligator Retrieval Device The device is intended for use in Recalled by...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN SMN 10699533 (500 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Antibacterial Hydrophilic Intermittent Catheter Recalled by C.R....
The Issue: Misbranding; the product labeled as an Antibacterial Hydrophilic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm Recalled...
The Issue: The Drager Pendula spring arm device has a set of screws located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN 10699201 (100 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory Adapter Part number 600525A0 Product Usage: designed for the...
The Issue: Maquet Inc. is initiating a voluntary field action on the Accessory Adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marathon Flow Directed Micro Catheter Recalled by Micro Therapeutics Inc,...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pipeline Embolization Device (Pipeline Classic) The device is indicated for...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN...
The Issue: The device defect is a positive bias of up to 20% relative to the currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normal Saline Flush 0.9% USP Sodium Chloride Injection Syringe Recalled by...
The Issue: Potential contamination with B. cepacia.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Practices kits containing certain production lots of Clearify...
The Issue: Product sterility is compromised due to breach of the sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-Quant Hemoglobin A1c Gen. 2 Hemoglobin A1c test Catalog number Recalled...
The Issue: Roche Diagnostics has confirmed elevated QC and patient sample recovery for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBAS INTEGRA 800 Tina-Quant Hemoglobin A1cDX Gen.2 Hemoglobin A1cDX test...
The Issue: .Roche Diagnostics has confirmed elevated QC and patient sample recovery for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Clearify Visualization System Item Code: 21-345 Intended to be...
The Issue: Product sterility is compromised due to breach of the sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm TI Calibrated Reaming Rod 850 mm Recalled by Synthes (USA) Products...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extraction Hook - Sterile for TI Cannulated Nails Recalled by Synthes (USA)...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod W/Ball Tip 650 mm Recalled by Synthes (USA) Products LLC...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 37751 Recharger Product Usage: The Medtronic 37751 Recharger is...
The Issue: Medtronic has identified an increased number of complaints from customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.