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

All Food Drug Medical Device Consumer Product Vehicle

Showing 24741–24760 of 51,038 recalls

Medical DeviceOctober 10, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: A problem has been detected in the Philips IntelliVue MX4O that, if it were...

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

Class II — Potential Health HazardOngoing

Medical DeviceOctober 10, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Naera Hospital Bassinet Recalled by Stryker Medical Division of Stryker...

The Issue: It was identified that the volume of air inside the mattress may expand in...

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

Class II — Potential Health HazardOngoing

FoodOctober 10, 2018· Quest Nutrition, LLC

Recalled Item: Quest Protein Bar Vanilla Almond Crunch Single Bar UPC# - Recalled by Quest...

The Issue: Undeclared allergen; tree nut (almonds)

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

Class III — Low RiskOngoing

Refund

FoodOctober 9, 2018· World Variety Produce Inc.

Recalled Item: Melissa's Hatch Chile Clean Snax Recalled by World Variety Produce Inc. Due...

The Issue: Firm discovered that Hatch Chile Clean Snax lists peanuts in the ingredient...

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

Class II — Potential Health HazardOngoing

Refund

Medical DeviceOctober 9, 2018· Synaptive Medical Inc

Recalled Item: BrightMatter Guide Recalled by Synaptive Medical Inc Due to This recall has...

The Issue: This recall has been initiated due to a software defect found in the Guide...

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

Class I — Serious Health HazardOngoing

Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 3K 2.5 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing

Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing

Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing

Medical DeviceOctober 9, 2018· Theragenics Corporation

Recalled Item: Theragenics Applicator Needle (18g x 20cm) The device is comprised Recalled...

The Issue: Some of the pouches containing Brachytherapy Applicator Needles (18g x 20cm)...

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

Class II — Potential Health HazardOngoing

DrugOctober 9, 2018· Sprayology

Recalled Item: Man Power Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...