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. 2,623 recalls have been distributed to Connecticut in the last 12 months.
Showing 9321–9340 of 51,038 recalls
Recalled Item: Safe tussin PM Recalled by Denison Pharmaceuticals, LLC Due to CGMP...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colic Calm Recalled by Denison Pharmaceuticals, LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safe tussin DM Recalled by Denison Pharmaceuticals, LLC Due to CGMP...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDLINE THERAHONEY GEL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline issued a recall on TheraHoney Wound Gel due to the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to Device...
The Issue: Device may experience malfunctions due to misalignment of the check valve in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TREO ABDOMINAL STENT-GRAFT SYSTEM (TREO) consists of four types of...
The Issue: Potential for the incorrect size stent-graft than the printed carton label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGACY SMARTBASE Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Non-engaging abutments were distributed without FDA clearance; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera 14 Gauge Biopsy Device-intended to obtain percutaneous core biopsy...
The Issue: The inner needle of the Sertera device is either detaching or discharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Sign Sensor 2 Recalled by SenTec AG Due to The sensors may experience an...
The Issue: The sensors may experience an out-of-box failure because after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine Tablets Recalled by Glenmark Therapeutics, Inc. Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength: some cartons labeled and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trilogy Evo O2 EV300 Recalled by Philips Respironics, Inc. Due to...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B Recalled by...
The Issue: IFU- Instructions for Use (IFU) package insert and both the IFU packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Environmental...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...
The Issue: The Trilogy Evo Universal ventilator provides continuous or intermittent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 and LifeVent EVO2 Recalled by Philips Respironics, Inc. Due...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: vasopressin 20 units added to 0.9% sodium chloride 100 mL* Recalled by...
The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.