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. 983 recalls have been distributed to Kentucky in the last 12 months.
Showing 36461–36480 of 51,386 recalls
Recalled Item: VP-CH-PNV PRENATAL/POSTNATAL Prescription Folic Acid-Containing Dietary...
The Issue: Defective Delivery System: Product may contain leaking capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by Bio-pharm, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Product recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by...
The Issue: Dove Chocolate Assortment Snowflakes may contain undeclared peanuts, what...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TWININGS OF London ENGLISH BREAKFAST BLACK TEA DECAFFEINATED Recalled by...
The Issue: Twinings English Breakfast Black Tea 12ct Kcups, were packaged in cartons...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cardiosave Hybrid and rescue IABP Recalled by Maquet Datascope Corp -...
The Issue: Maquet has recieved information that in some Cardiosave IABPS, the scroll...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF Recalled by Stryker...
The Issue: There were two potential interference conditions identified with the way the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...
The Issue: The door latch may not fully close and the door may open unexpectedly. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...
The Issue: On a rare occasion, there is a potential to assign a patient result to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...
The Issue: An issue with the Panorama Central Station may cause the system to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triple Ginger Brew Recalled by Trader Joes Company Due to Trader Joes...
The Issue: Trader Joes recalling Triple Ginger Brew due to reports of unopened bottles...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: XCEL Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared Fluoxetine
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: Infinity Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...
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: Asset extreme+PLUS Capsules Recalled by Bee Extremely Amazed LLC Due to...
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: Prime Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...
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.