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. 2,656 recalls have been distributed to Kentucky in the last 12 months.
Showing 3961–3980 of 51,386 recalls
Recalled Item: Dapsone Gel 7.5% Recalled by VIONA PHARMACEUTICALS INC Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: Ti Locking Cap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR Suture Anchors. Tendon/ligament Recalled by Smith & Nephew Inc....
The Issue: Sterile barrier breach due to inadequate packaging design that could not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Artificial Urinary Sphincter Control Pump Recalled by Boston Scientific...
The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Artificial Urinary Sphincter Pressure Regulating Balloon 61-70 cm H2O...
The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to Gradient...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w 3.0T Recalled by GE Medical Systems, LLC Due to Gradient...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to Gradient coils...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a...
The Issue: Due to incorrect labels applied to devices during servicing. Labels contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by Lannett Company Inc. Due to...
The Issue: Failed Content Uniformity Specifications: Product failed to meet the action...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Galaxy bronchoscope (Product GALB-001) used with Instructions for use...
The Issue: Not all biopsy tools meant to fit bronchoscope channel (2.1mm inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDO KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Identified...
The Issue: Identified lots of Olympus product may be missing sterile and manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERACARE Cold Hot Medicated Patch Recalled by Unexo Life Sciences Private...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ABSORBINE jr. Extra Large BACK PATCH Recalled by Unexo Life Sciences Private...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PARCHE LEON PAIN RELIEVING HOT PATCH Recalled by Unexo Life Sciences Private...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: THERACARE MAXIMUM STRENGTH PAIN RELIEF 4% LIDOCAINE PATCH Recalled by Unexo...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LILAS Feminine Pain Relief Patch Recalled by Unexo Life Sciences Private...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EQUATE MAXIMUM STRENGTH LIDOCAINE PAIN RELIEVING PATCH Lidocaine 4% Topical...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.