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 85018520 of 51,038 recalls

FoodJuly 13, 2023· Commercial Bakeries

Recalled Item: Trader Joe's Gluten Free Joe-Joe's Chocolate Vanilla Creme Sandwich Cookies...

The Issue: Undeclared peanut

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

Class III — Low RiskOngoing
Refund
FoodJuly 13, 2023· Commercial Bakeries

Recalled Item: Gluten Free MI-DEL Swedish Style Ginger Snaps Net Wt. 8 Recalled by...

The Issue: Undeclared peanut

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 13, 2023· EMPATICA SRL

Recalled Item: Embrace2- Indicated for use as an adjunct to seizure monitoring Recalled by...

The Issue: May have a battery life lasting less than the full 48 hours, requiring the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· Instrumentation Laboratory

Recalled Item: ACL TOP Family 50 Series Models as follows: In vitro Recalled by...

The Issue: Sample misidentification could occur under specific conditions and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Redwood 2.0 ultrasound systems Recalled by Siemens Medical Solutions...

The Issue: If a user-generated preset for an 18L6 transducer created on a 1.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to Lipemic interference...

The Issue: Lipemic interference failed to meet the performance specification listed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Olympus Corporation of the Americas

Recalled Item: The Air/Water Valve is provided/used with the following Endoscopes:...

The Issue: The air/water valve MAJ-1444 used with OER-Pro and OER-Elite may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX S Recalled by Medicrea International Due to There is a potential for a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX C+ Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Draeger Medical, Inc.

Recalled Item: Carina Sub-Acute Care Ventilator Recalled by Draeger Medical, Inc. Due to...

The Issue: Presence of polyether polyurethane (PE-PUR) and emission of...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: GRANVIA-C Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA+ Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX DLIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX 3D Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX TLIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: PASS LP Recalled by Medicrea International Due to There is a potential for a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF S/A Recalled by Medicrea International Due to There is a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Libre 2 Readers Recalled by Abbott Diabetes Care, Inc. Due to If...

The Issue: If blood glucose monitoring system users attempt to start a new sensor, when...

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

Class II — Potential Health HazardOngoing