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 13121–13140 of 27,899 recalls
Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit)-for IVD of folate Recalled by...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit )- for IVD Recalled by Siemens...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay Recalled...
The Issue: Assay files used on the open Dynex DSX Instrument to process IVD ELISA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge MCC Flow i Disposable CO2 absorber Recalled by GETINGE US SALES LLC...
The Issue: Reversed expiration and manufacturing date on the label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Enteral Safe Feeding Tubes: a) Recalled by DeRoyal Industries Inc...
The Issue: Certain MED-RX Polyurethane Feeding Tubes are being recalled due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NobelActive Internal NP 3.5x15mm Endosseus dental implant Recalled by Nobel...
The Issue: The top label for dental implant may incorrectly indicate the implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips 5-Lead Set Recalled by Philips North America, LLC Due to The...
The Issue: The thickness of the connector to the trunk cable on affected limb lead sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm FDR Go Plus mobile X-ray system Recalled by Fujifilm Medical...
The Issue: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYMUTEST HIA MonoStrip Recalled by Aniara Diagnostica LLC Due to Residual...
The Issue: Residual crystallization of the microplate and recurrent negative controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYMUTEST HIA MonoStrip Recalled by Aniara Diagnostica LLC Due to Residual...
The Issue: Residual crystallization of the microplate and recurrent negative controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central...
The Issue: Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IGuide System Recalled by Medical Intelligence Medizintechnik Gmbh Due to...
The Issue: Sometimes, although the HexaPOD has reached the target position, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autoject EI Recalled by Owen Mumford USA, Inc. Due to There is a possible...
The Issue: There is a possible assembly error on Autoject EI, lot number V14. This lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Petfine Auto Injector Recalled by Owen Mumford USA, Inc. Due to There is a...
The Issue: There is a possible assembly error on Autoject EI, lot number V14. This lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Enteric Viral Panel RUO Recalled by Becton Dickinson & Co. Due to...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max StaphSR Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 1 USA Recalled by Becton Dickinson & Co. Due to The foil...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit EXT Enteric Bacterial Panel Recalled by Becton Dickinson & Co. Due to...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Check-Points CPO IVD EU Recalled by Becton Dickinson & Co. Due to...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.