Product Recalls in Connecticut
Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,552 recalls have been distributed to Connecticut in the last 12 months.
Showing 13341–13360 of 28,245 recalls
Recalled Item: Kit BD Max MRSA 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 Vaginal Panel 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 BD Max ExK DNA 2 EU LUO Recalled by Becton Dickinson & Co. Due to The...
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 CT/GC/TV 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 Cdiff EU 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 GC RT PCR Assay Recalled by Becton Dickinson & Co. Due to The...
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 Enteric Parasite Panel EU Recalled by Becton Dickinson & Co. Due...
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 2 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 BD Max Enteric Bacterial Panel EU Recalled by Becton Dickinson & Co. Due...
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 MRSA XT 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 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: Philips Azurion systems with software version R1.2 -Interventional...
The Issue: The cold restart of Azurion R1.2 systems may take up to 7 minutes if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The...
The Issue: Non-conforming devices are identified, which may not have been included in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fukushima suction tubes Recalled by TeDan Surgical Innovations LLC Due to...
The Issue: There was incorrect raw material used in the production of the identified lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: xTAG Respiratory Viral Panel (RVP): Box Label: xTAG RVP (Respiratory...
The Issue: The Assay may give a false negative result when detecting and subtyping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage:...
The Issue: Negative Bias with Lot EA9227.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Pelvic Trainer (MPT) Recalled by Ralston Group Due to The device was...
The Issue: The device was incorrectly listed with the FDA and is therefore considered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.