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. 2,357 recalls have been distributed to New Hampshire in the last 12 months.
Showing 30681–30700 of 49,311 recalls
Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cryptococcal Antigen Lateral Flow Assay (CrAg LFA) Recalled by...
The Issue: The affected products have approximately a 91% specificity while the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Cisco 3850 layer 3 switch Recalled by Philips Electronics North...
The Issue: May experience a loss of centralized monitoring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...
The Issue: Endologix updated the Instructions for Use (IFU) and implemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...
The Issue: Endologix updated the Instructions for Use (IFU) and implemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number...
The Issue: Maquet has received 3 confirmed complaints related to the Li-lon Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OASIS DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation...
The Issue: Cross profile for Varian 60 degree wedge shows "horns."
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine Hydrochloride extended release capsules Recalled by Aurobindo...
The Issue: Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Furosemide Tablets USP Recalled by Roxane Laboratories, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: An unusually thick tablet was reported...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TEMAZEPAM CAPSULES USP Recalled by Vintage Pharmaceuticals LLC, DBA...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ambrosia Quality Foods Brand 4/1 gallon Worcestershire Sauce Net 128 Fl. Oz....
The Issue: Ambrosia brand 4/1 Gallon Worcestershire Sauce may contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.