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. 2,456 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,456 in last 12 months

Showing 2192121940 of 28,245 recalls

Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova 2121IQ. Angiographic X-ray systems used in generating...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Optima CL 323i. Angiographic X-ray systems used in Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· Tecan US, Inc.

Recalled Item: Infinite F500 Recalled by Tecan US, Inc. Due to A firmware bug causes...

The Issue: A firmware bug causes incorrect values to be displayed for specific measured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Discovery IGS 730. Angiographic X-ray systems used in Recalled...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova IGS 630. Angiographic X-ray systems used in Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· RAYSEARCH LABORATORIES AB

Recalled Item: Radiation Therapy Treatment Planning System software RayStation is a...

The Issue: An error caused by a floating point precision problem tends to cause a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Discovery IGS 740 & GE Healthcare Innova IGS Recalled by GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova IGS 620. Angiographic X-ray systems used in Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova 3100IQ. Angiographic X-ray systems used in generating...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Triathlon PS X3 Tibial Insert Recalled by Stryker Howmedica Osteonics Corp....

The Issue: Stryker Orthopaedics received a report that 5537-G-319 No 3. Triathlon TS...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· Tecan US, Inc.

Recalled Item: Infinite 200 in vitro diagnostic. Product Usage: The Tecan Infinite Recalled...

The Issue: A firmware bug causes incorrect values to be displayed for specific measured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova IGS 540. Angiographic X-ray systems used in Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: The PowerLED / X-TEN / VOLISTA Surgical Light Systems are Recalled by Maquet...

The Issue: Maquet Suspension Arms used with PowerLED/X-TEN/Volista Surgical Light...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...

The Issue: validation data related to cleaning instructions and sterilization methods...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Cleaver Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...

The Issue: validation data related to cleaning instructions and sterilization methods...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

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

Class II — Potential Health HazardOngoing