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. 2,672 recalls have been distributed to Kentucky in the last 12 months.
Showing 1841–1860 of 51,386 recalls
Recalled Item: ENDOTAK RELIANCE G/SG Recalled by Boston Scientific Corporation Due to...
The Issue: Affected lead models may experience gradually rising LVSI measurements in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Favorite Day Bakery Frosted Sugar Cookies Recalled by GIVE AND GO PREPARED...
The Issue: Foreign Material (wood)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: An out-of-Specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X1 Model RXM1000 UDI Codes: (01)00860003983812(11)230504(21)X11001...
The Issue: Due to incorrect software configuration that potentially allows more than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bartels ELISA Legionella Urinary Antigen. Model Number: B1029-440. In Vitro...
The Issue: Potential for Bartels ELISA Legionella Urinary Antigen kit B1029-440 lot 065...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Middlefield Original Cheese Co-op 100% Grass-Fed Pepper Jack Cheese...
The Issue: Potential contamination with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1) Middlefield Original Cheese Co-op Monterey Jack Cheese Recalled by...
The Issue: Potential contamination with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Paneer Cheese Recalled by Middlefield Original Cheese Cooperative Due to...
The Issue: Potential contamination with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Middlefield Original Cheese Co-op Horseradish Flavored Cheese Recalled by...
The Issue: Potential contamination with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Ascend Laboratories,...
The Issue: Failed Dissolution Specifications: low dissolution results
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Belsomra (suvorexant) tablets Recalled by Merck & Co. Inc Due to Failed...
The Issue: Failed Dissolution Specifications: potential for delayed dissolution of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: CELSITE Product Name: CELSITE BABYPORT SET PUR 4 Recalled by...
The Issue: The potential for minor injury such as damage to the vessel and/or tearing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Operated infusion pumps. t:slim X2 G5 Recalled by Tandem Diabetes...
The Issue: Insulin pumps manufactured with speakers from Revision A and B may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Satellite. Product Code: All . All software versions. The Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.