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. 1,087 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,087 in last 12 months

Showing 11301–11320 of 51,038 recalls

Medical DeviceNovember 7, 2022· R & D Systems, Inc.

Recalled Item: R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control...

The Issue: For one lot of CBC-3D Hematology Control, the Normal Level may exhibit...

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

Class III — Low RiskOngoing
FoodNovember 7, 2022· Betty Buzz LLC

Recalled Item: Betty Buzz Sparkling Grapefruit - Non-alcoholic Beverage & Mixer Container...

The Issue: Beverage has off-odor

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 5, 2022· Adam's Polishes LLC

Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...

The Issue: CGMP Deviations: Other lots of hand sanitizer are being recalled because...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 5, 2022· Adam's Polishes LLC

Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...

The Issue: Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 4, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan...

The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)-...

The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS...

The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Olympus Corporation of the Americas

Recalled Item: HF Resection Electrodes Recalled by Olympus Corporation of the Americas Due...

The Issue: An incompatible HF cable may be packaged with the HF Resection Electrodes....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2022· Icotec Ag

Recalled Item: VADER Pedicle System Torque Wrench Recalled by Icotec Ag Due to During...

The Issue: During internal testing (at manufacturer site) of two torque wrench devices,...

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

Class II — Potential Health HazardOngoing
FoodNovember 3, 2022· Nestle-USA, Inc. (Corporate Office)

Recalled Item: Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in Recalled by...

The Issue: Potential of foreign material within product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIP...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: Carefusion V. Mueller GERALD BIPOLAR FORCEPS 1.0MM WIDE TIP OVERALL Recalled...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller Neuro/Spine TITANIUM ROUND HANDLE BAYONET BIPOLAR...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS Recalled...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller ADSON BIPOLAR FORCEPS 1.0MM TIP Recalled by Carefusion...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: Carefusion V. Mueller SEMKIN BIPOLAR FORCEPS 1.5MM TIP Recalled by...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: Carefusion V. Mueller HARDY BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: Carefusion V. Mueller GERALD BAYONET BIPOLAR FORCEPS 1.0MM TIP Recalled by...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

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

Class II — Potential Health HazardOngoing