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. 2,579 recalls have been distributed to New Hampshire in the last 12 months.
Showing 1861–1880 of 49,311 recalls
Recalled Item: Blood/EMB Recalled by Remel, Inc Due to Potential Listeria Contamination
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bicillin L-A (penicllin G benzathine injectable suspension) Recalled by...
The Issue: CGMP Deviations; particulates identified during visual inspection
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bicillin L-A (penicillin G benzathine injectable suspension) Recalled by...
The Issue: CGMP Deviations; particulates identified during visual inspection
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beauty & Skincare Power Stick original nourishing invisible protection...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shave and Skincare Power Stick Original Nourishing Invisible Protection...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative Recalled by...
The Issue: FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MICRO-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All-round Joystick R-net Light. Electrical wheelchair component. Recalled by...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MULTI-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-ARLITE-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Description/ PYXIS MEDBANK MINI 1FH-1FM/169-137 Recalled by CareFusion 303,...
The Issue: Reports of delayed access to medication in automated dispensing cabinets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Thyroglobulin assay Recalled by Beckman Coulter, Inc. Due to Access...
The Issue: Access Thyroglobulin reagent lot 439163 may generate erroneously high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluorescein 2% Ophth Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Tablets 90 mg Recalled by Strides Pharma, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.