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. 2,664 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,664 in last 12 months

Showing 28412860 of 51,038 recalls

FoodMarch 10, 2025· NEW YORK WHOLESALE GROUP

Recalled Item: Zaarah Herbals brand Bhringraj Powder Recalled by NEW YORK WHOLESALE GROUP...

The Issue: Products contain elevated levels of Lead (Pb): 3.231 ppm and Arsenic (As):...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 10, 2025· NEW YORK WHOLESALE GROUP

Recalled Item: Zaarah Herbals brand Gurmar Powder Recalled by NEW YORK WHOLESALE GROUP Due...

The Issue: Products contain elevated levels of Lead (Pb): 3.688 ppm

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 10, 2025· NEW YORK WHOLESALE GROUP

Recalled Item: Zaarah Herbals brand Vasaka Powder Recalled by NEW YORK WHOLESALE GROUP Due...

The Issue: Products contain elevated levels of Lead (Pb): 6.504 ppm

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 10, 2025· NEW YORK WHOLESALE GROUP

Recalled Item: Zaarah Herbals brand Rasayan Churan Recalled by NEW YORK WHOLESALE GROUP Due...

The Issue: Products contain elevated levels of Lead (Pb): 88.038 ppm

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 10, 2025· Medtronic Xomed, Inc.

Recalled Item: NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 Recalled by...

The Issue: Nerve Monitoring System with certain software versions has potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Philips North America Llc

Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...

The Issue: Potential for collimator to fall as a result of incorrect installation.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Maquet Cardiovascular, LLC

Recalled Item: Maquet VH-3010 Power Supply. Used to deliver power to the Recalled by Maquet...

The Issue: Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2025· Philips North America Llc

Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...

The Issue: Potential for collimator to fall as a result of incorrect installation.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2025· Straumann USA LLC

Recalled Item: TLX/TLC SP Guided Implant Driver Recalled by Straumann USA LLC Due to The...

The Issue: The devices are missing the laser marked depth markings.

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

Class II — Potential Health HazardOngoing
DrugMarch 7, 2025· Direct Rx

Recalled Item: Duloxetine D/R Recalled by Direct Rx Due to CGMP Deviations: Presence of...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Direct Rx

Recalled Item: Duloxetine D/R Recalled by Direct Rx Due to CGMP Deviations: Presence of...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· ASEGUA THERAPEUTICS LLC

Recalled Item: Sofosbuvir and Velpatasvir Recalled by ASEGUA THERAPEUTICS LLC Due to...

The Issue: Defective Container: blister packs not properly sealed resulting in tablets...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Mylan Institutional, Inc.

Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...

The Issue: Super-Potent Drug: Out of specification potency results were obtained.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Slate Run Pharmaceuticals

Recalled Item: Cinacalcet Hydrochloride Tablets 60 mg Recalled by Slate Run Pharmaceuticals...

The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Mylan Institutional, Inc.

Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...

The Issue: Super-Potent Drug: Out of specification potency results were obtained.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Slate Run Pharmaceuticals

Recalled Item: Cinacalcet Hydrochloride Tablets 30 mg Recalled by Slate Run Pharmaceuticals...

The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing