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. 2,485 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,485 in last 12 months

Showing 2136121380 of 51,038 recalls

FoodSeptember 28, 2019· Adm Milling

Recalled Item: Bova Flour HG Recalled by Adm Milling Due to Potential E. coli Contamination

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2019· Adm Milling

Recalled Item: Sir Lancelot HG Flour Unbl Recalled by Adm Milling Due to Potential E. coli...

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2019· Adm Milling

Recalled Item: Polar Bear Flour UNTR /Prod Code: 710200 in 50# bags Recalled by Adm Milling...

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2019· Adm Milling

Recalled Item: Sir Galahad flour / Product Code: 805226 in 50# bags Recalled by Adm Milling...

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2019· Adm Milling

Recalled Item: Balancer flour 50 lbs bags Recalled by Adm Milling Due to Potential E. coli...

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2019· Adm Milling

Recalled Item: King Arthur All Purpose Flour 25# bags Recalled by Adm Milling Due to...

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 27, 2019· Images Unlimited Products, dba Cellect Products

Recalled Item: CELLECT brand and ESSENTIALS FACTOR Cell Synergy brand Unflavored Powdered...

The Issue: Product contains unsafe levels of Arsenic and Lead

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Arbor Pharmaceuticals Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by Arbor Pharmaceuticals Inc. Due...

The Issue: Labeling:Label Mix-up: Shipper Carton labelled Testosterone Cypionate...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2019· Epic Pharma, LLC

Recalled Item: Estradiol tablets Recalled by Epic Pharma, LLC Due to Presence of Foreign...

The Issue: Presence of Foreign Tablets/Capsules: Estradiol 1 mg was found in a 100...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2019· Alkermes, Inc.

Recalled Item: Vivitrol (naltrexone for extended-release injectable suspension) 380...

The Issue: Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version (IUO) 5.4 Catalog Number: A31774 Recalled...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 Recalled...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...

The Issue: Device was shipped without a Unique Device Identification (UDI) label.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System - Product Usage: Indicated for...

The Issue: Power supply (Model Number: TLC-2003) ME90A2403F01 (24 VDC, 3.75 A, 90 W, 1%...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version 5.8 Catalog Number:A36601 and A36602...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing