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. 1,739 recalls have been distributed to Connecticut in the last 12 months.
Showing 49501–49520 of 51,038 recalls
Recalled Item: SPECIALTY AUDIBLE TORQUE WRENCH Recalled by Stryker Spine Due to Multiple...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker XIA 3 TORQUE WRENCH Manufactured by: Stryker Recalled by Stryker...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biliary Catheters (Models A47XX and CB0XXXXX): Model Numbers & Description:...
The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmeriWater MRO Dialysis RO+ System Recalled by AmeriWater Inc Due to The...
The Issue: The firm was notified that a malfunction of the device was caused by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker MANTIS TORQUE WRENCH Manufactured by: Stryker pine Recalled by...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jaffe Bros. brand Recalled by Jaffe Brothers Due to Recall was initiated...
The Issue: Recall was initiated after firm was informed by their supplier Specialty...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Positron Emission Tomography (PET) and X-ray Computed Tomography Recalled by...
The Issue: Philips became aware of an issue relating to a UPS battery cabinet that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Devices includes a Multi Port Inflator or without Multi Port Recalled by...
The Issue: Parks Medical Electronics, Inc. was made aware of two incidents where an air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare conducted...
The Issue: GE Healthcare conducted a recall on various mobile x-ray units (Optima...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Prolactin Assay: ADVIA Centaur Calibrator B Catalog Number....
The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur FSH Assay: ADVIA Centaur Calibrator B US: Calibrator Recalled...
The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doxazosin Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Cross...
The Issue: Cross Contamination w/Other Products: During stability testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...
The Issue: Although the reported incidence is low, there is the potential for the drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically...
The Issue: The seat could break as a result of damage resulting from a seat belt being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Recalled by Stryker Howmedica Osteonics Corp....
The Issue: During the manufacturing of the affected lot a manufacturing error has led...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.