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. 1,667 recalls have been distributed to New Hampshire in the last 12 months.
Showing 46381–46400 of 49,311 recalls
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due...
The Issue: There is the potential of the residual moisture of the Diacap Ultra membrane...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bumble Bee Brand 5oz Chunk White Albacore in Water Recalled by Bumble Bee...
The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brunswick and Bumble Bee Brand 5oz Chunk Light Tuna in Water. Recalled by...
The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jasmine Brand Garlic Flavored Crackers (Krupuk Bawang) Recalled by Jans...
The Issue: Wira Corp. is recalling Jasmine Garlic Flavored Crackers because of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bumble Bee Brand 5oz Chunk Light Tuna in Vegetable Oil Recalled by Bumble...
The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Siemens Mammomat Inspiration - full-field digital mammography Product Usage:...
The Issue: Firm became aware of an unintended behavior when using the Mammomat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers :...
The Issue: Natus Neurology Incorporated is recalling the Nicolet EEG Wireless Amplifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirtex SIR-yttrium 90 microspheres (Radionuclide) Recalled by Sirtex Medical...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Venous blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is Recalled...
The Issue: Medtronic has found through device testing that if the optional footswitch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare PCA infusion system with Hospira MedNet software allows...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PCA 3 infusion pump allows clinicians Recalled by Hospira Inc. Due to...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.