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. 1,747 recalls have been distributed to New Hampshire in the last 12 months.
Showing 34061–34080 of 49,311 recalls
Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ adjust aluminum crutch under the following labels: 1) EZ Recalled by...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aluminum crutch under the following labels: 1) Aluminum crutch Recalled by...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The...
The Issue: Siemens found a defective part in their production line which could increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: The two sets of wires (4 total wires) exiting from the EMI filters were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Interlocking Bolt Recalled by Synthes (USA) Products LLC Due to...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...
The Issue: Presence of Particulate Matter: Glass particles found in the product after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.