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. 2,508 recalls have been distributed to New Hampshire in the last 12 months.
Showing 12021–12040 of 27,899 recalls
Recalled Item: Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product...
The Issue: Cases of Portex¿ Lumbar Puncture Tray Child, SKU #4826PL-20 had been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 Software Upgrade Kit Recalled by Abbott Due to Internal...
The Issue: Internal testing of software identified software anomaly scenarios where if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uDR 596i Digital Medical X-Ray Imaging System - Product Usage: Recalled by...
The Issue: Two issues were identified with the stationary x-ray system. 1. Some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Editing an assay Test Definition and switching to another assay s Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x4 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4oz. Tube Recalled by Gentell, Inc Due to During an FDA...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIO Soft Tissue Protector Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential for the NAVIO Soft Tissue Protector to become stuck or bound to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 2x2 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x8 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The CapsoCam Plus (SV-3) Recalled by Capso Vision, Inc. Due to Ingestible...
The Issue: Ingestible video capsule system has capsule with incorrect capture mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A...
The Issue: Philips has received a number of reports of HeartStart MRx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nexus Universal with OptiBond Universal Recalled by Kerr/Pentron, DBA Kerr...
The Issue: An issue within production process used to package trial kits let to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder...
The Issue: Distributed without an approved 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction)...
The Issue: Distributed without an approved 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LivaNova Heater-Cooler System 3T - Product Usage: The Heater-Cooler 3T...
The Issue: The firm is providing validated cleaning and disinfection instructions in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496...
The Issue: Incorrect expiration date on introduction cannula packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124...
The Issue: Incorrect expiration date on introduction cannula packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmniSure ROM Test Recalled by Qiagen Sciences LLC Due to An image on the...
The Issue: An image on the associated polybag contains an incorrect rinse time of 30...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCM4 Base unit Recalled by Radiometer Medical ApS Due to Reports have been...
The Issue: Reports have been received about the transcutaneous monitoring system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avalon Elite Vascular Access Kit Recalled by Maquet Cardiovascular Us Sales,...
The Issue: A lot of Avalon Elite Vascular Access Kits (VAK) are being recalled due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.