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. 2,408 recalls have been distributed to Connecticut in the last 12 months.
Showing 36841–36860 of 51,038 recalls
Recalled Item: TATE'S BAKE SHOP CHOCOLATE CHIP COOKIES Recalled by Tate's Wholesale, Llc....
The Issue: Tate's Bake Shop has recalled Chocolate Chip Cookies and Ginger Zinger...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Conte's Gluten Free Wheat Free Cheese Ravioli Net Wt. 12 Recalled by Contes...
The Issue: This recall has been initiated due to possible contamination with Salmonella...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Metro Brand Irresistibles Gluten Free Cheese Ravioli with Marinara Sauce...
The Issue: This recall has been initiated due to possible contamination with Salmonella...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Conte's Gluten Free Wheat Free Cheese Ravioli With Marinara Sauce Recalled...
The Issue: This recall has been initiated due to possible contamination with Salmonella...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Metro Irresistibles Gluten Free Cheese Ravioli 6- 9 ounce bags Use By 020317...
The Issue: This recall has been initiated due to possible contamination with Salmonella...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kozy Shack Indulgent Salted Caramel Recalled by Land O' Lakes, Inc Due to...
The Issue: Kozy Shack is recalling one lot of Kozy Shack Indulgent Recipe Pudding in a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thin-Flex Venous Cannula Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Edwards Lifesciences initiated a field action for the Thin-Flex Venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Copper NiTi Preformed Archwires Recalled by Ormco/Sybronendo Due to Ormco...
The Issue: Ormco Corporation is recalling Copper NiTi Preformed Archwires because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (CE-IVD) Recalled by Diagnostic Hybrids, Inc. Due...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (RUO) Recalled by Diagnostic Hybrids, Inc. Due to A...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue CIC-C1q EIA Recalled by Diagnostic Hybrids, Inc. Due to A component...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK Recalled by...
The Issue: Procedure Products initiated the recall due to the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT Recalled by...
The Issue: Procedure Products initiated the recall due to the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT Recalled by...
The Issue: Procedure Products initiated the recall due to the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER Recalled by...
The Issue: Procedure Products initiated the recall due to the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS V3000 Recalled by Philips Electronics North America Corporation Due...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS CV Recalled by Philips Electronics North America Corporation Due to...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.