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 23881–23900 of 49,311 recalls
Recalled Item: Thyroveev Recalled by Hellolife Due to Microbial Contamination of Non...
The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Compulsin Recalled by Hellolife Due to Microbial Contamination of Non...
The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neuroveen Recalled by Hellolife Due to Microbial Contamination of Non...
The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva...
The Issue: One lot of the specified needles is not performing as intended due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-360 Analyzer Recalled by Tosoh Bioscience Inc Due to The firm has...
The Issue: The firm has implemented new product labeling changes for the Tosoh AIA-360...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Recalled...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp :...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 12mm SpinDown Clamp Recalled by Zimmer...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters Recalled by Smiths...
The Issue: Several lots of Jelco¿ ViaValve" safety intravenous (I.V.) catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp Recalled...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp :...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to The...
The Issue: The catheter failed the endotoxin testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyroid Powder 25kg/drum Recalled by Sichuan Friendly Pharmaceutical...
The Issue: CGMP Deviations: Thyroid Powder has inconsistent levels of the active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.