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. 2,476 recalls have been distributed to New Hampshire in the last 12 months.
Showing 14661–14680 of 27,899 recalls
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software...
The Issue: software malfunction; It was found when a user performs radiography using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in Recalled by ASO, LLC...
The Issue: Potential that gauze pads may not be fully sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion¿ Model 4000 Syringe Infusion Pump Recalled by Smiths Medical ASD...
The Issue: Customers who utilize PharmGuard¿ Server Software (PGS) with Medfusion¿ 4000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...
The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Total T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...
The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Compress Devices and Instruments: Item Number/Item Description 178350...
The Issue: Correction to update the surgical technique for the Compress System. To make...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE Recalled by Atrium Medical...
The Issue: This recall has been initiated in response to a seal defect found in certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical InfinityTM DBS System 8CH Directional Lead Recalled by St....
The Issue: The most proximal unsegmented electrode of the Deep Brain Stimulation leads,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge Recalled...
The Issue: Siemens Healthcare Diagnostics has confirmed that Dimension Vista Lactate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naera Hospital Bassinet Recalled by Stryker Medical Division of Stryker...
The Issue: It was identified that the volume of air inside the mattress may expand in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: A problem has been detected in the Philips IntelliVue MX4O that, if it were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FR3 Defibrillator Recalled by Philips Electronics North...
The Issue: Automated external defibrillators may not fully meet IPx5 water ingress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Theragenics Applicator Needle (18g x 20cm) The device is comprised Recalled...
The Issue: Some of the pouches containing Brachytherapy Applicator Needles (18g x 20cm)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg Recalled by...
The Issue: Discolored powder has confirmed the presence of a foreign substance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg Recalled by...
The Issue: Discolored powder has confirmed the presence of a foreign substance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.