Product Recalls in Kentucky
Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,002 recalls have been distributed to Kentucky in the last 12 months.
Showing 29981–30000 of 51,386 recalls
Recalled Item: Straight Shank Drill Bit 4.0 mm Diameter Recalled by Zimmer Biomet, Inc. Due...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill 4.5 mm Diameter (.177 Inch) Recalled by...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Distal Drill Pilot Tip 3.2 mm Diameter Recalled...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Periarticular Locking Plate System Locking Screw Tap Standard...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill Bits 3.2 mm Diameter (.126 Inch)...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Freehand Drill 4.3 mm Diameter 152.5 mm Length...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill 1.5 mm Diameter (.059 Inch) Recalled by...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Bit Quick-Connect 1.5 mm Diameter 85 mm Length Recalled by Zimmer...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MULTIGENT Creatinine (Enzymatic) Recalled by Sentinel CH SPA Due to Reagent...
The Issue: Reagent 1 component may result in Quality Control values shifting out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROMETRA II Programmable Infusion Pump Recalled by Flowonix Medical, Inc....
The Issue: Flowonix Medical received a report of a patient implanted with the Prometra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended...
The Issue: Olympic Pasteurmatic 3000/3500 Systems are recalled because they do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech 1.5" Novation Calcar Planer Guide Tip To assist the Recalled by...
The Issue: The firm determined that the labeling (surgical technique) should be updated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Caffeine Powder Recalled by Global Marketing Enterprises, Inc. Due to...
The Issue: Marketed without an Approved NDA/ANDA: The product consists of pure,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biotech Underground Tri-Ton Hardcore Formula capsules Recalled by DYNAMIC...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare LightSpeed VCT X-ray system Recalled by GE Healthcare, LLC Due...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery NM/CT 670 CZT X-ray system Recalled by GE...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.