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. 1,729 recalls have been distributed to Kentucky in the last 12 months.
Showing 43941–43960 of 51,386 recalls
Recalled Item: Super ARTHGOLD 500mg Recalled by Sung Soo Kim Due to Undeclared Indomethacin
The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxandrolone Tablets Recalled by Upsher Smith Laboratories, Inc. Due to...
The Issue: Labeling: Missing Label; Three cases of product (total of 36 bottles) were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Day Time Cold & Flu Recalled by P&L Developments, LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Phenylephrine component is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HALOPERIDOL DECANOATE INJECTION Recalled by Fresenius Kabi USA LLC Due to...
The Issue: Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM Tablets Recalled by Golden State Medical Supply Inc. Due...
The Issue: Presence of Foreign Substance; some bottles may contain debris that was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TX1 Tissue Removal System. TX1 Procedure Pack P/N 554-1003-001 (outer box)...
The Issue: The sterile barrier in the packaging may be compromised due to cracks in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...
The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Laureate 0.035" (0.89mm) Hydrophilic Guide Wire Recalled by Merit...
The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Laureate Hydrophilic Guide Wire Recalled by Merit Medical Systems,...
The Issue: Discrepancy between the carton and unit labeling for the Merit Laureate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...
The Issue: A stock check revealed broken glass fibers between the connector and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ Percutaneous Sheath Introducer Kits The Percutaneous sheath...
The Issue: Arrow is recalling the Arrow¿ Percutaneous Sheath Introducer Kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Organic traditions DARK CHOCOLATE SACHA INCHI SEEDS***DAIRY & SUGAR FREE...
The Issue: Undeclared milk allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic traditions DARK CHOCOLATE GOLDEN BERRIES***DAIRY & SUGAR FREE 80%...
The Issue: Undeclared milk allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PRIVATE SELECTION SWEET STRAWBERRY SORBET Recalled by Kroger Co Due to...
The Issue: The firm was notified of the presence of undeclared milk in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jolly Time Microwave popcorn Recalled by American Pop Corn Co Due to The...
The Issue: The product has the potential to be contaminated with stainless steel metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jolly Time Microwave popcorn Recalled by American Pop Corn Co Due to The...
The Issue: The product has the potential to be contaminated with stainless steel metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jolly Time Microwave popcorn Recalled by American Pop Corn Co Due to The...
The Issue: The product has the potential to be contaminated with stainless steel metal...
Recommended Action: Do not consume. Return to store for a refund or discard.