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 15411560 of 51,038 recalls

Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Lumina (DE). Model Number: 11344916. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number:...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217. Recalled by Siemens...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396 Recalled by...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Vida Fit. Model Number: 11410481. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra fit. Model Number: 10849580. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Cima.X (DE). Model Number: 11647158. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio Dot Upgrade. Model Number: 10684334. Recalled by Siemens...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Connectom.X. Model Number: 11371480. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio Dot. Model Number: 10684333. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Boston Scientific Corporation

Recalled Item: Extractor Pro RX Retrieval Balloon Catheter Recalled by Boston Scientific...

The Issue: The product in incorrectly labeled. The label indicates that the skive hole...

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

Class II — Potential Health HazardOngoing
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: Lantiseptic Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: KleenFoam Antimicrobial Foam Soap Recalled by DermaRite Industries, LLC Due...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: DermaFungal Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: DermaSarra Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: PeriGiene Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: DermaMed Ointment Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: PeriGuard Ointment Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: Renew PeriProtect Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: DermaKleen Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund