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. 2,529 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,529 in last 12 months

Showing 1810118120 of 51,038 recalls

FoodSeptember 23, 2020· Hale And Hearty Soups, LLC

Recalled Item: WILD MUSHROOM BARLEY soup Recalled by Hale And Hearty Soups, LLC Due to...

The Issue: Product may contain pieces of maggots.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 22, 2020· Flexicare Medical Ltd.

Recalled Item: ProVu Single Use Video Stylet with ET Tube Recalled by Flexicare Medical...

The Issue: When the video stylet cuff is over-inflated there is potential for occlusion...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 22, 2020· Cardinal Health 200, LLC

Recalled Item: Kangaroo Connect 1000ml Bag Set Recalled by Cardinal Health 200, LLC Due to...

The Issue: The feeding spike sets may leak at the interface of the tube and spike...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Cardinal Health 200, LLC

Recalled Item: Kangaroo Connect 500ml Bag Set Recalled by Cardinal Health 200, LLC Due to...

The Issue: The feeding spike sets may leak at the interface of the tube and spike...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Gordian Surgical

Recalled Item: TroClose 1200 - Product Usage: intended for use in a variety of gynecologic...

The Issue: Endotoxin test results found above the acceptable levels in LAL test (above...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Pentax of America Inc

Recalled Item: 9372HD Digital Capture (ver. 1.1.0 + w/ 9263 endoPortal) Recalled by Pentax...

The Issue: There is an intermittent software issue that could affect the systems, in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Boston Scientific Corporation

Recalled Item: Visual-ICE MRI Cryoablation System Mobile Connection Panel (Visual-ICE MRI...

The Issue: Incorrectly installed base.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Pentax of America Inc

Recalled Item: 9310HD Digital Video Capture Module with software version 3.4.0 or Recalled...

The Issue: There is an intermittent software issue that could affect the systems, in...

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

Class II — Potential Health HazardOngoing
FoodSeptember 21, 2020· Wismettac Asian Foods, INC

Recalled Item: Shirakiku brand Black Fungus (Kikurage) Recalled by Wismettac Asian Foods,...

The Issue: California Department of Public Health sampled and tested Shirakiku brand...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 21, 2020· Stereotaxis Inc

Recalled Item: Niobe ES System Recalled by Stereotaxis Inc Due to There is a potential for...

The Issue: There is a potential for fire in the inside computer cabinet.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· Smith & Nephew, Inc.

Recalled Item: 5.5MM Arthrogarde Hip Access Cannula Recalled by Smith & Nephew, Inc. Due to...

The Issue: The J Lock feature on the cannula body was manufactured incorrectly,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· GE Healthcare, LLC

Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to There is a potential...

The Issue: There is a potential for a smudge artifact that could be suspect for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray...

The Issue: Potential malfunction in which the examination room monitor may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· Stryker Neurovascular

Recalled Item: Trevo XP ProVue Retriever Recalled by Stryker Neurovascular Due to Increase...

The Issue: Increase in fracture complaints of the flexible, tapered core wire,...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 21, 2020· Smith & Nephew, Inc.

Recalled Item: Genesis (GII) - Product Usage: designed for use in patients Recalled by...

The Issue: The anterior locking detail does not meet its design specifications.

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

Class II — Potential Health HazardOngoing
FoodSeptember 19, 2020· Dianne's Fine Desserts

Recalled Item: Devonshire Bake Shop brand Lemon Italian Cream Cake Recalled by Dianne's...

The Issue: Product contains undeclared peanuts.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 18, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage:...

The Issue: There is a software problem which affects the DSA Roadmap application on...

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

Class II — Potential Health HazardOngoing
DrugSeptember 17, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 15 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: FDA analysis found these products to be less than the...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 17, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 120 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent...

The Issue: Subpotent Drug: FDA analysis found these products to be less than the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 17, 2020· Genicon, Inc.

Recalled Item: A Li-Gator Single Use Laparoscopic Clip Applier Recalled by Genicon, Inc....

The Issue: Device malfunction causing the applier to jam, and clip loading failures.

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

Class II — Potential Health HazardOngoing