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. 900 recalls have been distributed to Kentucky in the last 12 months.
Showing 50741–50760 of 51,386 recalls
Recalled Item: FX PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT- DR OWEN Product Usage: The Sarns Cardioplegia Recalled by...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED TRANSPLANT PACK Product Usage: The Sarns Cardioplegia Cannula and...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XC HEART/LUNG PACK W/SX25RX Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED H/L PK W/FX15RW40 Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT-DR GERHARDT Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYO MN XCOATED 3/8X1/2 AV Product Usage: The Sarns Cardioplegia Recalled by...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS ANTEGRADE: CARDIOPLEGIA CANNULA: ROOT INFUSION VENT/CATHETER WITH 14-...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dent's Extra Strength Toothache Gum Recalled by Grandpa Brands Co Due to...
The Issue: Superpotent; benzocaine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The product has the Catalogue/Part number 60010. Olympic Cool-Cap System...
The Issue: The Olympic Cool-Cap's Control Module has experienced a frozen screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Recalled by Hill...
The Issue: Subpotent; fluocinolone acetonide
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morton Recalled by Morton Salt Co. Due to Impurities/Degradation Products:...
The Issue: Impurities/Degradation Products: The product was found to contain a slightly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Topical Oil (Scalp Oil)...
The Issue: Subpotent; fluocinolone acetonide
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12...
The Issue: Siemens Healthcare Diagnostics has confirmed that the presence of Intrinsic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panera Recalled by Panera Bread LLC Due to Product ingredient statement...
The Issue: Product ingredient statement reversed for Reduced Fat Honey Walnut Cream...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen Oysters Recalled by Seoul Shik Poom, Inc. Due to Korean Certified...
The Issue: Korean Certified Shippers delisted from ICSSL.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen Salted Clam Recalled by Seoul Shik Poom, Inc. Due to Korean Certified...
The Issue: Korean Certified Shippers delisted from ICSSL.
Recommended Action: Do not consume. Return to store for a refund or discard.