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. 2,370 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,370 in last 12 months

Showing 4200142020 of 51,038 recalls

FoodSeptember 24, 2014· Original Soup Man

Recalled Item: THE ORIGINAL SOUPMAN Lobster Bisque Recalled by Original Soup Man Due to...

The Issue: The Original Soup Man has recalled Lobster Bisque due to the presense of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 24, 2014· Philips Medical Systems, Inc.

Recalled Item: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector...

The Issue: Loss of key image functionality due to a bent pedal of the Footswitch.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2014· Philips Medical Systems, Inc.

Recalled Item: Foot Switches used with the following systems: Philips Allura Xper Systems...

The Issue: Loss of key image functionality due to a bent pedal of the Footswitch.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2014· Straumann USA, LLC

Recalled Item: Straumann Bone Level Implant 04.1 mm RC Recalled by Straumann USA, LLC Due...

The Issue: Product transfer piece was fitted with a Narrow Connect (NC) instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: siemens Dimension¿ Phenytoin Flex¿ Reagent Cartridge The PTN method used...

The Issue: Internal testing has confirmed a low absorbance range between the levels 1...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2014· Joerns Healthcare

Recalled Item: Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed...

The Issue: The Easy-Care Care-Lock feature installed at the foot of the bed may...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2014· Biomet, Inc.

Recalled Item: Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety...

The Issue: An investigation identified that the product was incorrectly manufactured as...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2014· Invacare Corporation

Recalled Item: Invacare Perfecto 2 V Oxygen Concentrator The finished device is Recalled by...

The Issue: It was determined that a defective sieve bed subassembly enabled zeolite...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego systems Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A cable inside the C-arm systems may have been routed in an inappropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2014· Virtual Imaging, Inc.

Recalled Item: Digital Mobile X-ray Systems used to take diagnostic radiographic exposures...

The Issue: There is a potential for unintended and erratic motion.

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

Class II — Potential Health HazardOngoing
FoodSeptember 19, 2014· United Natural Trading

Recalled Item: 1) Nature's Place Organic Campfire Trail Mix Recalled by United Natural...

The Issue: The various trail mixes may contain undeclared cashew kernels.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 19, 2014· Mars Chocolate North America

Recalled Item: Mars Chocolate North America Milk Chocolate M & M's Net Recalled by Mars...

The Issue: Mars Chocolate North America is recalling M & Ms due to undeclared peanuts.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE /IMMULITE 1000 Systems COR Cortisol Recalled by Siemens Healthcare...

The Issue: Customer complaints were received for positive bias reported on the controls...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: External power supply adaptors that accompany Clinitek Status+ The Clinitek...

The Issue: The external power supply for the Clintek Status analyzer, which is provided...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: External power supply adaptors that accompany Clinitek Status Connect System...

The Issue: The external power supply for the Clintek Status analyzer, which is provided...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: External power supply adaptors that accompany Clinitek Status Power Supply...

The Issue: The external power supply for the Clintek Status analyzer, which is provided...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Carescape Patient Data Module Recalled by GE Healthcare, LLC...

The Issue: GE Healthcare has recently become aware of a potential safety issue to the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 18, 2014· Bracco Diagnostic Inc

Recalled Item: E-Z- GAS II EFFERVESCENT GRANULES Antacid/Antiflatulent Recalled by Bracco...

The Issue: Subpotent Drug: Out of Specification (OOS) result during routine stability...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number:...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing