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. 2,442 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,442 in last 12 months

Showing 3106131080 of 51,038 recalls

Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology A PICC permits venous access Recalled...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow VPS Access Kit with Maximal Barrier Precautions for use Recalled by...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit. The...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath Recalled...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow¿ Access Kit with Maximal Barrier Precautions for use with Recalled by...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit The large-bore multiple-lumen...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arterial Line Kit with Sharps Safety Features and Maximal Barrier Recalled...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
DrugMarch 20, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: CLENZIderm M.D. Acne Treatment System Recalled by Valeant Pharmaceuticals...

The Issue: Discoloration.

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

Class III — Low RiskOngoing
Refund
DrugMarch 20, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment 5 fl. oz. (148...

The Issue: Discoloration.

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

Class III — Low RiskOngoing
Refund
DrugMarch 20, 2017· G & W Laboratories, Inc.

Recalled Item: Ciclopirox Olamine Cream USP Recalled by G & W Laboratories, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: product lots packaged with an...

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

Class III — Low RiskOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluocinonide Cream UPS Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Cross contamination with other products: Certain lots of Fluocinonide Cream...

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

Class III — Low RiskOngoing
Refund
DrugMarch 17, 2017· Akorn, Inc.

Recalled Item: LATANOPROST OPHTHALMIC SOLUTION Recalled by Akorn, Inc. Due to Lack of...

The Issue: Lack of assurance of sterility: product was found to be empty, under-filled,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2017· Shire

Recalled Item: Kalbitor (ecallantide) Recalled by Shire Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: Glass

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

Class II — Potential Health HazardOngoing
Refund