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. 1,032 recalls have been distributed to Connecticut in the last 12 months.
Showing 18401–18420 of 51,038 recalls
Recalled Item: Whole Foods Market Artequeso Manchego 6 month aged raw Raw Recalled by Whole...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market Chimay Grand Cru PLU 29388800000 and Whole Recalled by...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market Chimay Biere PLU 29351700000 Individual sliced cheese...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Market Mitica La Dama Sagrada Raw Milk - Recalled by Whole Foods...
The Issue: Undeclared lysozyme (from egg whites)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HIGH LINER FOODSERVICE***Genuine Maryland-Style Premium Crab Cakes***48-3...
The Issue: Product contains undeclared hydrolyzed soy protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Just Hand Sanitizer (Ethyl Alcohol 73%) Single Use-Packs 100-count NDC...
The Issue: Labeling Not Elsewhere Classified: Product labeled to contain methanol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol) Recalled...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ Recalled by Open...
The Issue: Labeling Not Elsewhere Classified: Product labeled to contain methanol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh Bioscience AIA- PACK HCG Calibrator Set-In Vitro Diagnostic for...
The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) Recalled by Maquet...
The Issue: Instruction For Use (IFU) incorrect serial number of 90437000. It should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh Bioscience AIA-PACK BHCG Calibration Verification Test Set-In Vitro...
The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Module (dual...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot)...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent)...
The Issue: Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carl Zeiss Meditec AG VISUREF150 - Product Usage: Recalled by Carl Zeiss...
The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carl Zeiss Meditec Ag VISULENS 550 - Product Recalled by Carl Zeiss Meditec...
The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...
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: 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: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...
The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.