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. 1,008 recalls have been distributed to Kentucky in the last 12 months.
Showing 27381–27400 of 51,386 recalls
Recalled Item: Intra-Aortic Balloon Catheter Mega 8FR 50cc Product Usage: The intra-aortic...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 with 4.1.7 XX026 software version model number 728231 Recalled...
The Issue: Surview scan with tube current lower than 30 mA is unable to be initialized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: F-T3SYSTEM Recalled by Allen Medical Systems Due to The recalling firm has...
The Issue: The recalling firm has become aware that the rail section clamps used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 125II Assay Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Upon dilution, some patient samples may exhibit over-recovery outside the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 7.5FR 40cc Product Usage: The...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 56% 1 Day Silicone Hydrogel (-2.50) Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emerald brand Glazed Walnuts Recalled by Snyder's-Lance Inc. Due to...
The Issue: Snyder's Lance is voluntarily recalling 6.5 oz. Emerald brand walnuts due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atropine Sulfate Ophthalmic 1% Solution Recalled by Akorn, Inc. Due to...
The Issue: Failed Stability Specification: OOS low viscosity results discovered during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: True 3D Viewer Recalled by Echopixel, Inc. Due to With certain software...
The Issue: With certain software versions, import of enhanced ultrasound formatted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Labetalol Hydrochloride Injection Recalled by Hospira Inc. A Pfizer Company...
The Issue: Defective Container: Cracked glass at the rim surface of glass vials,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza software Syngo.Plaza is a Picture Archiving and Communication...
The Issue: Software upgrade to correct format of study dates and issues with Legacy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza software VB10A model numbers: 10863171 Recalled by Siemens...
The Issue: Software upgrade to correct format of study dates and issues with Legacy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotte Kancho Choco-Biscuit Recalled by Lotte International America Corp. Due...
The Issue: Firm was notified by customer of peanut allergen found in the product during...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable...
The Issue: Lack of adequate validation and controls to ensure that product cleanliness...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini...
The Issue: Lack of adequate validation and controls to ensure that product cleanliness...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strauss Penis Clamp 130MM/General Instruments Recalled by Aesculap Implant...
The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.