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. 1,032 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,032 in last 12 months

Showing 19241–19260 of 51,038 recalls

DrugMay 15, 2020· Eco Lips Inc

Recalled Item: EcoLips Sport Lip Balm Recalled by Eco Lips Inc Due to Superpotent Drug: The...

The Issue: Superpotent Drug: The active ingredient, avobenzone, is used at 5% which is...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2020· TRIOVA PHARMACEUTICALS LLC

Recalled Item: Estriol USP Micronized 5 G Recalled by TRIOVA PHARMACEUTICALS LLC Due to...

The Issue: Failed impurities/ degradation specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics Inc.

Recalled Item: Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer...

The Issue: Flexible tubing connected to the liquid waste bottle can crack during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Mediana Co., Ltd.

Recalled Item: DIRECT SUPPLY Attendant VITAL SIGNS MONITOR Recalled by Mediana Co., Ltd....

The Issue: Failures were found in the temperature measurement function while in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: (1) CentraLink Data Management System software version 16.0.2 Siemens...

The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics Inc.

Recalled Item: Siemens IMMULITE 2000 XPi Immunoassay System - In vitro Chemistry Recalled...

The Issue: Flexible tubing connected to the liquid waste bottle can crack during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: (1) Atellica Data Manager software version 1.0 Siemens Material Number...

The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 7 HOLE 140MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. T15 LOW PROFILE CORTICAL SCREW 3.5mm x 28mm Recalled by Biomet Due...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: Biomet 8.0 Cannulated Screw Tap-Bone fixation screw Item Number: 110008467...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Neocis Inc.

Recalled Item: DRW-0742-01: Gen 2 Anterior Chairside Splint LLUR (lower left-upper right)...

The Issue: The LRUL and LLUR posterior chairside splints and LLUR anterior chairside...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE RIGHT 11 HOLE 190MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing