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. 2,529 recalls have been distributed to Connecticut in the last 12 months.
Showing 18421–18440 of 51,038 recalls
Recalled Item: Talladium Luminesse Zirconia Discs Recalled by Talladium Inc Due to The...
The Issue: The linear shrinkage on the zirconia blank disc s part label is incorrect....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS Recalled by Merge Healthcare, Inc. Due to Measurements done on...
The Issue: Measurements done on the Merge PACS generated MPR s may have incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Command Brands GelAnti Bac Instant Hand Sanitizer Recalled by ROQUE PLAST,...
The Issue: CGMP Deviation: Potential contamination with undeclared methanol.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) 0.5 FL OZ (15 mL) bottles...
The Issue: cGMP Deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Day & Night Pack Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) Recalled by...
The Issue: cGMP Deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by PAI Holdings, LLC. dba Pharmaceutical...
The Issue: Subpotent drug: Out of specification for assay at the 15-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ear Pain MD Pain Relief Drops with 4% Lidocaine (lidocaine Recalled by...
The Issue: cGMP Deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ear Pain MD Pain Relief Drops For Kids (lidocaine HCl Recalled by Eosera,...
The Issue: cGMP Deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to Tube trays may leak...
The Issue: Tube trays may leak which could invalidate patient results or assay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Padgett Dermatome Set - Product Usage: are intended for Recalled by...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 ft Handpiece Cable Recalled by Integra LifeSciences Corp. Due to lntegra...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Padgett Electric Dermatome Set - Product Usage: are intended...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris System PC Unit Model 8100 (Pump Module) and Recalled by CareFusion...
The Issue: Pump Module keypad may exhibit keys that are unresponsive or stuck as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015 Recalled by CareFusion 303, Inc. Due to The...
The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris System Recalled by CareFusion 303, Inc. Due to The Alaris PC unit...
The Issue: The Alaris PC unit can display incorrect syringe type and/or syringe sizes....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PC Unit Front Case with Keypad Replacement Kits: TC10008389 ASSY Recalled by...
The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.