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 26161–26180 of 51,386 recalls
Recalled Item: Cheerios Protein Oats & Honey Recalled by General Mills, Inc Due to...
The Issue: Cheerios Protein Oats and Honey cereal may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AMPI Whey Powder Recalled by AMPI Due to Potential Salmonella Contamination
The Issue: Whey powder may have the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: utz Carolina Style Barbeque Potato Chips Recalled by Utz Quality Food Inc...
The Issue: Utz¿ Quality Foods, LLC., is voluntarily recalling select expiration dates...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Haemonetics OrthoPAT System-Integrated Set. Product Code: 1150H-00 OrthoPAT...
The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS3 Vital Signs Monitor Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VM 3/4/6/8 Patient Monitors Recalled by Philips...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VSV (Vital Signs Viewer) Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin...
The Issue: The product was mislabeled with the incorrect label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HEMODIALYSIS SYS Recalled by Fresenius Medical Care Renal Therapies...
The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HEMODIALYSIS SYSTEM W/BIBAG Recalled by Fresenius Medical Care Renal...
The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS4 Vital Signs Monitor Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G8 Automated HPLC Analyzer - 723G8 Product Usage - In Recalled by Tosoh...
The Issue: Analyzers were distributed with software which lacks a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS2 monitor Recalled by Philips Electronics North America...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code:...
The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution...
The Issue: Immersion time stated on the bottle is 45 minutes while the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by Sun Pharmaceutical Industries,...
The Issue: Presence of Particulate Matter: organic and inorganic compounds detected in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Double Lumen CRRT/ABP Catheter Set Recalled by Medical Components, Inc dba...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duo-Flow IJ Full Tray Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOFT-LINE DUO-FLOW DOUBLE LUMEN CATHETER/CATHETER SET Recalled by Medical...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Recalled by...
The Issue: Dental varnish has the possibility of having an unpleasant and off flavor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.