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. 2,445 recalls have been distributed to Connecticut in the last 12 months.
Showing 23881–23900 of 28,245 recalls
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gel-E Donut Recalled by Childrens Medical Ventures Due to The gel-filled...
The Issue: The gel-filled Gel-E Donut and Squishon product line has received a number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shape HF Cardiopulmonary System. Made up of Shape HF System Recalled by...
The Issue: Shape Medical has initiated a correction due to a mandatory software upgrade...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FirmArray Blood Culture Identification (BCID) Panel Recalled by BioFire...
The Issue: BioFire has identified an increased risk of false positive results when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheters Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner catheter of some Langston V2 Dual Lumen Catheters have separated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint 500 Measurement Clinical Chemistry System RAPIDPoint 500...
The Issue: RAPIDPoint 500 Measurement Cartridges may have an error code one or more...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Recalled by Elekta, Inc. Due to When using CMA, if the user hovers the...
The Issue: When using CMA, if the user hovers the mouse pointer exactly above the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Potential loss of airway...
The Issue: Potential loss of airway gas measurement in the Compact Airway Gas Modules....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Although the Natural Rubber Latex...
The Issue: Although the Natural Rubber Latex caution symbol is clearly displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Reduced Neck Standard & Extended Offset Recalled by Zimmer,...
The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Cardiovascular Systems Recalled by Cardiovascular Systems, Inc. Due to...
The Issue: CSI has initiated a recall on the Diamondback 360 Peripheral Orbital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Hip Stem Standard & Extended Offset Recalled by Zimmer,...
The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology Recalled by Zimmer,...
The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns D4 Aortic Arch Cannulae 6.0mm Recalled by Terumo Cardiovascular...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Two-stage Venous Return Cannulae 32/40 & 36/51 Fr with Recalled by...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Flexible Aortic Arch Cannula 8.0mm with luer Recalled by Terumo...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Venoatrial Cannulae 36/46 Fr with 1/2" flare or connector Recalled by...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.