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. 1,825 recalls have been distributed to Kentucky in the last 12 months.
Showing 32181–32200 of 51,386 recalls
Recalled Item: DIAMONDBACK 360 Peripheral 1.50 Classic Recalled by Cardiovascular Systems...
The Issue: CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta International SA Recalled by Medacta Usa Inc Due to Damaged...
The Issue: Damaged packaging, lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Fixed Hinge Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentasa (mesalamine) Controlled-Release Capsules Recalled by Shire PLC Due...
The Issue: Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Derby City Vending Buffalo Chicken Sandwich Deli Selections Ingredients:...
The Issue: The firm failed to declare milk, egg & soy on their label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: A1CNow SELF CHECK (European) Recalled by Polymer Technology Systems Due to A...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Health At Home A1C Test Kit Recalled by Polymer Technology Systems Due...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A1CNow+ Systems (professional use product) Recalled by Polymer Technology...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReliOn FastA1C Test Recalled by Polymer Technology Systems Due to A...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walgreens At-Home A1C Test Kit Recalled by Polymer Technology Systems Due to...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Radiology 12.2 - Picture Archive Communication System (PACS)...
The Issue: Issue for customers that use an EMR login or legacy web URL login or legacy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...
The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.