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. 1,677 recalls have been distributed to New Hampshire in the last 12 months.
Showing 42301–42320 of 49,311 recalls
Recalled Item: Smiths Medical HOTLINE¿ Fluid Warming Set L-70. Product Usage: intended...
The Issue: Injection port of the Set may leak blood/ IV fluids from the septum of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Economy Elastic Knee Sleeve Open Recalled by Breg Inc Due to Breg is...
The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Lite Knee 2 Stays with Visco Recalled by Breg Inc Due to Breg is recalling...
The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPRIV¿ (velaglucerase alfa for injection) Recalled by Shire Human Genetic...
The Issue: Presence of Particulate Matter; Particulates identified as stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Natural Recalled by Smiley National Inc Due to Smiley National is...
The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Enhanced Bali Leaf Powder Recalled by Smiley National Inc Due to Smiley...
The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Enhanced Maeng Da Leaf Powder Recalled by Smiley National Inc Due to Smiley...
The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Natural Bali Kratom 40 Recalled by Smiley National Inc Due to Smiley...
The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merit Custom Syringe Kit Recalled by Merit Medical Systems, Inc. Due to The...
The Issue: The products are labeled as sterile but were not sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring Tubing Recalled by Merit Medical Systems, Inc. Due to...
The Issue: The products are labeled as sterile but were not sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas c8000 Modular Analyzer Series Cobas c502 Recalled by Roche Diagnostics...
The Issue: The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REUMOFAN PLUS Tablets Recalled by Pain Free By Nature Due to Undeclared...
The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Perrigo Recalled by Paddock Laboratories, LLC Due to Presence of Particulate...
The Issue: Presence of Particulate Matter Perrigo is recalling seven lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Suture Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Standard Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm x 100mm Weck Vista Universal Cone Open Access Recalled by...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port Short Length (53mm)...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck¿ Recalled by Teleflex Medical Due to Complaints were received...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mm Weck Vista Cannula-only Recalled by Teleflex Medical Due to Complaints...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.