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. 2,367 recalls have been distributed to New Hampshire in the last 12 months.
Showing 28661–28680 of 49,311 recalls
Recalled Item: Mefenamic Acid Recalled by Shionogi Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PONSTEL (Mefanamic Acid) USP Recalled by Shionogi Inc. Due to Failed...
The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mefenamic Acid Capsules Recalled by Shionogi Inc. Due to Presence of foreign...
The Issue: Presence of foreign substance: The recall was initiated due to black...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SHIMADZU FDR Visionary Catalog Number: FDR Visionary Suite Stationary x-ray...
The Issue: Cracks may occur over time on the tube holding shaft near the base of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIMADZU RADspeed Pro Catalog Number: RADspeed Pro Recalled by Shimadzu...
The Issue: Cracks may occur over time on the tube holding shaft near the base of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number:...
The Issue: Cracks may occur over time on the tube holding shaft near the base of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Video Gastroscope Recalled by Pentax of America Inc Due to Error...
The Issue: Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Video Gastroscope Recalled by Pentax of America Inc Due to Error...
The Issue: Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Diagnostics LeadCare Ultra and LeadCare Plus test Kits. Product...
The Issue: Underestimates the lead concentration of venous blood samples when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Diagnostics LeadCare and LeadCare II test Kits. Product Usage:...
The Issue: Underestimates the lead concentration of venous blood samples when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Protein 1 Control M Recalled by Siemens Healthcare...
The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Protein 1 Control H Recalled by Siemens Healthcare...
The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Protein 1 Calibrator Recalled by Siemens Healthcare...
The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Protein 1 Control Recalled by Siemens Healthcare...
The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROMETRA II Programmable Infusion Pump Recalled by Flowonix Medical, Inc....
The Issue: Flowonix Medical received a report of a patient implanted with the Prometra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MULTIGENT Creatinine (Enzymatic) Recalled by Sentinel CH SPA Due to Reagent...
The Issue: Reagent 1 component may result in Quality Control values shifting out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Bit Quick-Connect 1.5 mm Diameter 85 mm Length Recalled by Zimmer...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill 1.5 mm Diameter (.059 Inch) Recalled by...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Freehand Drill 4.3 mm Diameter 152.5 mm Length...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill Bits 3.2 mm Diameter (.126 Inch)...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.