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 26421–26440 of 28,245 recalls
Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Inline Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20-Pole Eco Cable Recalled by Biosense Webster, Inc. Due to Biosense is...
The Issue: Biosense is recalling the 20-Pole Eco Cable because it was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo.plaza SW version VA20 with Mammography license. image...
The Issue: Siemens issued a Customer Safety Notice to inform customers of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Connect QLC1677E Recalled by Steris Corporation Due to During a...
The Issue: During a routine label review, the firm identified four SYSTEM 1E Quick...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz Dual series CT Scanner System Recalled by Philips And Neusoft Medical...
The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sepp Recalled by CareFusion 213, LLC Due to An internal review of...
The Issue: An internal review of CareFusion's labeling for preoperative skin prep...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Multi-Slice CT Scanner System Recalled by Philips And Neusoft...
The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse...
The Issue: The product specifications sheet, part of the Instructions for Use (IFU),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir Recalled...
The Issue: Certain lots of Reagent reservoirs, may not have a separation in the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due...
The Issue: There is the potential of the residual moisture of the Diacap Ultra membrane...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mammomat Inspiration - full-field digital mammography Product Usage:...
The Issue: Firm became aware of an unintended behavior when using the Mammomat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is Recalled...
The Issue: Medtronic has found through device testing that if the optional footswitch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PCA 3 infusion pump allows clinicians Recalled by Hospira Inc. Due to...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare PCA infusion system with Hospira MedNet software allows...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers :...
The Issue: Natus Neurology Incorporated is recalling the Nicolet EEG Wireless Amplifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.