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. 1,976 recalls have been distributed to Kentucky in the last 12 months.
Showing 12681–12700 of 51,386 recalls
Recalled Item: ELITE MINI CARAMEL NET WT. 6.7OZ (190 g). Passover Bar Recalled by ELITE...
The Issue: Potential contamination with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ELITE GRAPE GUM WITH SUGAR NET WT. 2.32 (66 g) Recalled by ELITE...
The Issue: Potential contamination with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ELITE WHITE CHOCOLATE BAR & 815871012799. Net Wt. 3.53 Recalled by ELITE...
The Issue: Potential contamination with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ELITE PESEK ZMAN WAFER ROLL NET WT. 1.4 oz (40g) Recalled by ELITE...
The Issue: Potential contamination with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ELITE MILK CHOCOLATE COATED RICE CAKES NET WT 2.47OZ (70 g) Recalled by...
The Issue: Potential contamination with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Macadamia Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 Recalled by...
The Issue: Products may potentially contain one or more of the following undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Honeymoons Dark Chocolate Pecan. PLU Code: 788394 14720 3. Recalled by Queen...
The Issue: Products may potentially contain one or more of the following undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: X80 RADiant Photoelectric Therapy System Recalled by Xstrahl Limited Due to...
The Issue: There is a potential compatibility issue with the systems and replacement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GaviLyte -C (Polyethylene Glycol 3350 Recalled by Lupin Pharmaceuticals Inc....
The Issue: Failed Stability Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: In-Line ventilator adaptor Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential of reduced oxygenation or pneumothorax/barotrauma to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Wet -Field Eraser Recalled by Beaver Visitec International, Inc. Due to...
The Issue: Boxes labeled as Wet-Field Eraser, 18GA Blunt Tip, 45Deg., were shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEG 5000 Functional Fibrinogen Reagent Recalled by Haemonetics Corporation...
The Issue: Due to a shift in the citrated blood range for a normal population, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-Line ventilator adaptor Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential of reduced oxygenation or pneumothorax/barotrauma to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V2.x. Recalled by CardioTek BV Due to Device...
The Issue: Device did not pass electrical safety testing for adequate insulation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Back up batteries in Avance CS2 and Avance CS2 Pro Recalled by GE...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Field replacement back up batteries distributed on or after April 1 Recalled...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zonisamide Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin HCl 1.5 g in 0.9% Sodium Chloride Recalled by SCA Pharmaceuticals...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.