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. 2,485 recalls have been distributed to Connecticut in the last 12 months.
Showing 18641–18660 of 28,245 recalls
Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upper Torso Tray Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ortho Pack Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasal Pack Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Open Procedure Pack Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Varlock Cage/Trial Implant Holder Recalled by Kiscomedica S.A. Due to Firm...
The Issue: Firm received a complaint of the tip holder breaking during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumbar Laminectomy Pack Recalled by Windstone Medical Packaging, Inc. Due to...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Basic Pack (1185) Recalled by Windstone Medical Packaging, Inc. Due to The...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri GYN Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...
The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a Recalled...
The Issue: Ortho Kinematics Inc. sent a Notice of Correction to Released Testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr PS Knee Tibial Insert Recalled by Encore Medical, Lp Due to The...
The Issue: The Empowr PS Insert was reported as missing the impaction slot feature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The...
The Issue: Lima Proximal Bodies were inadvertently re-sterilized. The safety screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Sterilization System Recalled by Advanced Sterilization Products...
The Issue: Advanced Sterilization Products (ASP) has identified that in a rare sequence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GN200 Caiman HF generators Recalled by Aesculap Implant Systems LLC Due to...
The Issue: Generators may have a faulty component which could impact the proper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laerdal Compact Suction Unit ¿ 4 under the following labels: Recalled by...
The Issue: The On/Off functionality in the LCSU 4 is controlled by electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller...
The Issue: The Controller Cap of the C2 CyroBalloon Ablation System may crack as it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes various orthopedic instruments modified by U.S. Distributors...
The Issue: Products were made outside of Quality System Regulation, and potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.