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. 2,623 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,623 in last 12 months

Showing 76417660 of 51,038 recalls

FoodOctober 19, 2023· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Pumpkin Spice Waffles Recalled by Nature'S Path Foods...

The Issue: undeclared peanut

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 19, 2023· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Dark Chocolate Chip Waffles Recalled by Nature'S Path...

The Issue: undeclared peanut

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 19, 2023· Abbott Laboratories

Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...

The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Abbott Laboratories

Recalled Item: Alinity c Processing Module The Alinity c Processing Recalled by Abbott...

The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Abbott Laboratories

Recalled Item: ARCHITECT c4000 Processing Module 02P24-02 02P24-40 01R24-56 01R25-56...

The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc NXS Host Blood Analysis System Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed a potential issue that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Cardinal Health Clean Stool Transportation System-For the collection...

The Issue: Due to a manufacturing defect, certain Para-Pak vials may be at risk for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Para-Pak Zn-PVA/10% Formalin-for the routine collection Recalled by Meridian...

The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Para-Pak Clean Vial-For the collection Recalled by Meridian Bioscience Inc...

The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit - For access to the subarachnoid Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial access kit (without Prep solutions) Bit and Guard-For...

The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· CardioQuip, LLC

Recalled Item: CardioQuip Modular Cooler-Heater Recalled by CardioQuip, LLC Due to There is...

The Issue: There is a potential for the heating-chamber to malfunction resulting in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· CardioQuip, LLC

Recalled Item: CardioQuip Modular Cooler-Heater Recalled by CardioQuip, LLC Due to There is...

The Issue: There is a potential for the heating-chamber to malfunction resulting in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit -For access to the subarachnoid space Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit- For access to the subarachnoid space Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing