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. 1,087 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,087 in last 12 months

Showing 11481–11500 of 51,038 recalls

Medical DeviceOctober 17, 2022· Visionsense, Ltd.

Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope...

The Issue: Broken Optical fiber cable damage can occur through handling or bending and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2022· Steris Corporation

Recalled Item: GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to...

The Issue: Two electronic diode components (D1 & D4) placed in the reverse orientation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2022· Insulet Corporation

Recalled Item: 18239: ASM Omnipod Dash PDM Recalled by Insulet Corporation Due to The firm...

The Issue: The firm has become aware of PDM battery issues, including battery swelling,...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2022· Visionsense, Ltd.

Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam...

The Issue: Broken Optical fiber cable damage can occur through handling or bending and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2022· Visionsense, Ltd.

Recalled Item: VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2022· Sonendo Inc

Recalled Item: GentleWave System Posterior CleanFlow Procedure Instrument with Matrices...

The Issue: Procedure Instruments with erroneous unit carton labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2022· Sonendo Inc

Recalled Item: GentleWave System APM Procedure Instrument with Matrix Recalled by Sonendo...

The Issue: Procedure Instruments with erroneous unit carton labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2022· Medtronic Navigation, Inc.

Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER...

The Issue: Due to a defect in the outer pouch sterile seal

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2022· Getinge Usa Sales Inc

Recalled Item: Extension Tabletop for Operating Table System 1140 Recalled by Getinge Usa...

The Issue: The back rest may unintentionally drop suddenly, resulting in adverse health...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2022· Spectranetics Corporation

Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to Laser...

The Issue: Laser System may detect Error 106 or Error 108 System Failures that will...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Calibrator Kit 9 -(GEN) 22 of VITROS Recalled by...

The Issue: Calibration disk Data Release Version (DRV) 6194 to 6200 contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2022· Becton Dickinson & Co.

Recalled Item: BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for Recalled by...

The Issue: Misformulated minocycline-can cause erroneously increased Minimal Inhibitory...

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

Class II — Potential Health HazardOngoing
FoodOctober 13, 2022· Hammond's Candies Since 1920 II, LLC

Recalled Item: Hammond's Salted Caramel Cookies Recalled by Hammond's Candies Since 1920...

The Issue: Peanut Butter Chocolate Chip Cookies mispacked in Salted Caramel Cookies Box...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 13, 2022· Akorn, Inc.

Recalled Item: AK-POLY-BAC brand of Bacitracin cand Polymixin B Sulfate Ophthalmic Ointment...

The Issue: CGMP Deviations:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 13, 2022· Akorn, Inc.

Recalled Item: ERYTHROMYCIN OPHTHALMIC OINTMENT USP 0.5% Recalled by Akorn, Inc. Due to...

The Issue: CGMP Deviations:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 13, 2022· Akorn, Inc.

Recalled Item: PAREMYD (hydroxyamphetamine hydrobromide/ tropicamide ophthalmic solution)...

The Issue: CGMP Deviations:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 13, 2022· Akorn, Inc.

Recalled Item: Neomycin and Polymyxin B Sulfates Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 13, 2022· Akorn, Inc.

Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 13, 2022· Akorn, Inc.

Recalled Item: Proparacaine Hydrochloride Ophthalmic Solution Recalled by Akorn, Inc. Due...

The Issue: CGMP Deviations:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 13, 2022· Akorn, Inc.

Recalled Item: Olopatadine HCL Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund