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. 2,380 recalls have been distributed to New Hampshire in the last 12 months.
Showing 22861–22880 of 49,311 recalls
Recalled Item: Losartan Potassium Tablets Recalled by MAJOR PHARMACEUTICALS Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PageWriter TC70 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/o trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 w/trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 w/o trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC20 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insufflation tubing to be used with varies insufflator units. Recalled by...
The Issue: The sterile single-use tubing may contain higher ethylene oxide (EO)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC50 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nelaton Urinary Catheter Recalled by ConvaTec, Inc Due to An internal...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Feeding Tube Metric Recalled by ConvaTec, Inc Due to An internal assessment...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/ trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC50 Government Bundle Recalled by Philips North America, LLC Due...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilterFlow Suction Handle CH24 Recalled by ConvaTec, Inc Due to An internal...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forceps Blue Recalled by ConvaTec, Inc Due to An internal assessment of...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...
The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...
The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Entry Set Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal Posterior Stabilized (PS) Knee Replacement System Recalled by...
The Issue: The labeling of the boxes and sterile pouches did not match the contents.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical...
The Issue: Complaints of the snare loop not completely retracting and/or misshaping of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.