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. 2,625 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,625 in last 12 months

Showing 1148111500 of 13,398 recalls

DrugApril 25, 2014· Prestige Brands Holdings

Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...

The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 24, 2014· Baxter Healthcare Corp.

Recalled Item: Famotidine Injection 20 mg Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Baxter Healthcare Corporation has received a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2014· Teva Pharmaceuticals USA

Recalled Item: QVAR¿ (beclomethasone dipropionate HFA) Recalled by Teva Pharmaceuticals USA...

The Issue: Defective Delivery System; defective valve

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2014· SigmaPharm Laboratories LLC

Recalled Item: Liothyronine Sodium Tablets Recalled by SigmaPharm Laboratories LLC Due to...

The Issue: Cross Contamination with Other Products: Four lots of Liothyronine Sodium...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2014· Hospira Inc.

Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter: Confirmed customer complaint of discolored...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 21, 2014· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Nylon fibers found in a bottle of 0.9%...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2014· Hospira Inc.

Recalled Item: 1% LIDOCAINE HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer complaint that orange and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2014· Apotex Corp.

Recalled Item: Olanzapine Orally Disintegrating Tablets 5 mg Recalled by Apotex Corp. Due...

The Issue: Subpotent Drug: Out of specification (OOS) results at the 9 month...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 17, 2014· Trigen Laboratories, Inc.

Recalled Item: Triveen - PRx RNF Capsules Recalled by Trigen Laboratories, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Label indicates that the product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 17, 2014· Wockhardt Usa Inc.

Recalled Item: Wockhardt Metoprolol Succinate Recalled by Wockhardt Usa Inc. Due to Failed...

The Issue: Failed Dissolution Specifications: Product was out of specification (OOS) at...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 17, 2014· Cubist Pharmaceuticals, Inc.

Recalled Item: CUBICIN (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter: Customer complaint stating that one vial...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 16, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg Recalled by Pfizer...

The Issue: Presence of Foreign Tablets/Capsules: Pfizer is recalling 50 mg Pristiq...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2014· Sung Soo Kim

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.

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2014· P&L Developments, LLC

Recalled Item: Children's Triacting Night Time Cold & Cough with PE (diphenhydramine...

The Issue: Presence of Precipitate: Small amounts of diphenydramine and mannitol...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 14, 2014· P&L Developments, LLC

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.

Class III — Low RiskOngoing
Refund
DrugApril 14, 2014· Upsher Smith Laboratories, Inc.

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.

Class III — Low RiskOngoing
Refund
DrugApril 14, 2014· Golden State Medical Supply Inc.

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.

Class II — Potential Health HazardOngoing
Refund
DrugApril 14, 2014· Fresenius Kabi USA LLC

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.

Class III — Low RiskOngoing
Refund