State

Kentucky product recalls

73,381 recalls have nationwide distribution and so reach Kentucky. 7,197 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total: 7,197
Critical: 1,409
Severe: 2,024
Most recent: 2026-10-07

Of the 7,197 recalls naming Kentucky we have scored against our rubric, 1,409 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,024 (28%) are Severe.

Which agencies issued them

These figures cover only the 7,197 recalls whose distribution notice names Kentucky specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18976–19000 of 80578

ModerateFDA (Drugs)·D-0161-2023·2023-01-25
Triamterene and Hydrochlorothiazide Capsules Recalled for Failed Quality Specifications
Lannett Company is recalling Triamterene and Hydrochlorothiazide Capsules nationwide because the medication failed quality testing for impurity and degradation specifications. The recall affects 20,040 bottles.
Product
Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ] Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC 100 Count bottle: 0527-1632-01; NDC 1,000 bottle: 0527-1632-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0150-2023·2023-01-25
Antihistamine eye drops recalled due to manufacturing process deviations
Akorn, Inc. is recalling 163,996 bottles of Olopatadine HCl Ophthalmic Solution 0.1% due to manufacturing process deviations. Affected lot numbers expire from October through December 2023.
Product
Olopatadine HCl Ophthalmic Solution, USP 0.1%, 5 mL (0.17 FL OZ) per bottle, Antihistamine and Redness Reliever, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC: 51407-499-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0148-2023·2023-01-25
Ophthalmic solution recalled due to manufacturing quality control deviations
Akorn, Inc. is recalling 1,752 bottles of Olopatadine HCL Ophthalmic Solution, USP 0.1% nationwide due to manufacturing quality control deviations. Lot 1L03A with expiration 10/31/2023 is affected.
Product
Olopatadine HCL Ophthalmic Solution, USP 0.1%, Antihistamine and Redness Reliever, 5 mL (0.17 FL OZ) per bottle, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-308-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0134-2023·2023-01-25
Akorn Artificial Tears Eye Drops Recalled for Manufacturing Quality Deviations
Akorn, Inc. is voluntarily recalling 967,075 bottles of Artificial Tears Solution eye drops nationwide due to manufacturing process deviations identified during quality inspections.
Product
Artificial Tears Solution, Lubricant Eye Drops, Polyvinyl Alcohol 1.4%, 15 mL (0.5 fl. oz.) per bottle, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-060-12
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0145-2023·2023-01-25
FDA recalls Akorn ophthalmic ointment for manufacturing process deviations
Akorn, Inc. is recalling 2,082 tubes of Neomycin and Polymyxin B Sulfates, and Bacitracin Zinc Ophthalmic Ointment nationwide due to manufacturing process deviations. The recall is voluntary and initiated by the manufacturer.
Product
Neomycin and Polymyxin B Sulfates, and Bacitracin Zinc Ophthalmic Ointment, USP, Net Wt. 3.5 g (1/8 oz.), Rx Only, Manufactured by: Akorn, INC., Lake Forest, IL 60045. NDC: 17478-235-35
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0136-2023·2023-01-25
Ciprofloxacin ophthalmic solution recalled for manufacturing practice deviations
Akorn, Inc. is recalling 1,584 bottles of Ciprofloxacin Ophthalmic Solution nationwide due to Current Good Manufacturing Practice (CGMP) deviations. This is a voluntary recall.
Product
Ciprofloxacin Ophthalmic Solution, USP 0.3% (Ciprofloxacin HCl), 2.5mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-714-25
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0149-2023·2023-01-25
Olopatadine HCl ophthalmic solution recalled for manufacturing deviations
Olopatadine HCl Ophthalmic Solution 0.2% manufactured by Akorn, Inc. is being recalled nationwide due to Current Good Manufacturing Practice (CGMP) deviations affecting 173,928 bottles.
Product
Olopatadine HCl Ophthalmic Solution, USP 0.2%, 2.5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-305-12
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0162-2023·2023-01-25
Levofloxacin Tablets Recalled for Embossing and Packaging Insert Mismatch
Macleods Pharma USA recalls Levofloxacin Tablets 500 mg due to mismatched embossing on tablets versus the package insert labeling. The distributed bottles do not match the documented tablet markings.
Product
Levofloxacin Tablets, USP 500 mg; 50-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540; Manufactured by: Macleods Pharmaceuticals Ltd., Baddi, Himachal Pradesh, India. NDC 33342-022-08
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0164-2023·2023-01-25
Hand Sanitizer Recalled Due to Manufacturing Practice Deviations
Fisher Scientific voluntarily recalls hand sanitizer due to manufacturing deviations. The recall affects products distributed after March 31, 2022.
Product
Hand Sanitizer, HSANI4LI, (Isopropyl Alcohol), 75% Topical Solution, packaged in 4 L bottles, Thermo Fisher Scientific: Janssen Pharmaceuticalaan 3a, 2440 Geel - Belgium, 1 Reagent Lane, Fair Lawn, NJ 07410.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0163-2023·2023-01-25
Hand Sanitizer Recalled for Manufacturing Practice Deviations
Fisher Scientific voluntarily recalls HSANI500ML hand sanitizer (75% isopropyl alcohol) due to manufacturing practice deviations. The product was made under expired temporary FDA approval.
Product
Hand Sanitizer, HSANI500ML, (Isopropyl Alcohol), 75% v/v, packaged in a) 500 mL bottle and b) 6 x 500 mL bottles per case, Thermo Fisher Scientific: Janssen Pharmaceuticalaan 3a, 2440 Geel - Belgium, 1 Reagent Lane, Fair Lawn, NJ 07410.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0140-2023·2023-01-25
FDA recalls GONAK ophthalmic drug solution for manufacturing deviations
Akorn voluntarily recalled 196,254 bottles of GONAK ophthalmic solution nationwide due to CGMP manufacturing practice deviations. This professional-use eye solution is employed in gonioscopic examinations.
Product
GONAK Hypromellose Ophthalmic Demulcent Solution, (25 mg) 2.5%, 15 mL per dropper bottle, For Professional Use in Goinoscopic Examinations, Mfd. by: Akorn, INc., Lake Forest, IL 60045. NDC: 17478-064-12
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0137-2023·2023-01-25
FDA Recalls Cromolyn Sodium Eye Drops Nationwide for Manufacturing Defects
Akorn, Inc. is recalling 188,550 bottles of Cromolyn Sodium Ophthalmic Solution nationwide due to manufacturing quality control deviations.
Product
Cromolyn Sodium Ophthalmic Solution, USP 4%, 10mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-291-11
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0142-2023·2023-01-25
Akorn recalls Levofloxacin eye drops due to manufacturing compliance issues
Akorn, Inc. is recalling Levofloxacin Ophthalmic Solution due to manufacturing process deviations. The voluntary recall affects 3,108 bottles distributed nationwide.
Product
Levofloxacin Ophthalmic Solution 0.5%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, Il 60045. NDC: 17478-106-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0144-2023·2023-01-25
Akorn Recalls Moxifloxacin Ophthalmic Solution for CGMP Deviations
Akorn, Inc. is recalling 2,563 bottles of Moxifloxacin Ophthalmic Solution nationwide due to manufacturing deviations. The recall is voluntary and affects lot 1E28A with expiration date 4/30/2023.
Product
Moxifloxacin Ophthalmic Solution, USP, 0.5%, 3 mL per dropper bottle, Rx only, Manufactured by: Akorn, Lake Forest, IL 60045. NDC: 17478-519-19
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0146-2023·2023-01-25
Ofloxacin Ophthalmic Solution Recalled Nationwide for Manufacturing Quality Issues
Akorn, Inc. is recalling Ofloxacin Ophthalmic Solution 0.3% due to manufacturing quality deviations. The recall affects 65,006 bottles distributed nationwide.
Product
Ofloxacin Ophthalmic Solution, USP 0.3%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045; Distributed by: MWI, Boise, ID 83705. NDC: 13985-602-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0154-2023·2023-01-25
Drug recall: Proparacaine eye solution due to manufacturing deviations
Akorn, Inc. is recalling Proparacaine Hydrochloride Ophthalmic Solution due to manufacturing process deviations. The voluntary recall affects 23,026 bottles distributed nationwide.
Product
Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5%, 15 mL per bottle, Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Distributed By: MWI Boise, ID 83705, NDC: 13985-611-15
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0160-2023·2023-01-25
Triamterene and Hydrochlorothiazide Capsules Recalled for Failed Quality Specifications
Lannett Company is recalling Triamterene and Hydrochlorothiazide Capsules nationwide because certain lots failed impurity and degradation quality specifications. Consumers taking affected lots should consult their pharmacist or physician.
Product
Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, 1000 Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC: 0527-1632-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0167-2023·2023-01-25
SINUVA Sinus Implant Recalled for Failed Drug Release Specification
Intersect ENT, Inc. is recalling 9,898 pouches of SINUVA sinus implants nationwide after detecting failed drug release specifications during stability testing. The implant may not deliver the medication as intended.
Product
SINUVA — SINUVA (MOMETASONE FUROATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0138-2023·2023-01-25
Drug Recall: Erythromycin Ophthalmic Ointment Due to Manufacturing Deviations
Akorn, Inc. recalls 1.1 million tubes of Erythromycin Ophthalmic Ointment nationwide due to manufacturing deviations. The voluntary, Class II recall was initiated by the firm.
Product
ERYTHROMYCIN OPHTHALMIC OINTMENT USP 0.5%, Net Weight: 3.5g (1/8 oz) per tube, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-070-35
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0151-2023·2023-01-25
Prescription eye drop recall due to manufacturing compliance issues
Akorn, Inc. is recalling Olopatadine HCl Ophthalmic Solution due to manufacturing process deviations. The nationwide voluntary recall involves 121,176 bottles distributed across the United States.
Product
Olopatadine HCl Ophthalmic Solution, USP 0.1%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC: 60429-957-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0155-2023·2023-01-25
Sodium Chloride Ophthalmic Ointment Recalled for Manufacturing Deviations
Akorn, Inc. has voluntarily recalled 524,506 tubes of Sodium Chloride Ophthalmic Ointment, USP 5%, nationwide due to Current Good Manufacturing Practice deviations.
Product
Sodium Chloride Ophthalmic Ointment, USP, 5%, Net Wt. 3.5 g (1/8 oz.) per tube, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-622-35
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·23V024000·2023-01-23
Mack Recalls LRBE Electric Trucks Due to Cabin Heater Relay Fire Risk
Mack Trucks is recalling 2019 and 2021-2023 LRBE electric trucks because a failing cabin heater relay can cause the coolant heater to overheat, increasing the risk of fire.
Product
MACK — MACK LRBE (ELECTRIC)
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V023000·2023-01-23
Autocar Recalls Trucks Due to Parking Brake Release Risk
Autocar is recalling specific trucks because a worn parking brake valve may cause the brake to release unexpectedly, increasing the risk of a crash.
Product
AUTOCAR — AUTOCAR XPEDITOR, WXLL, WX, XPERT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V022000·2023-01-23
2021 Lincoln Aviator rearview camera video output may fail
Ford is recalling 2021 Lincoln Aviators with 360-degree camera systems because the rearview camera video may fail to display, reducing driver rear visibility and increasing crash risk.
Product
LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER, CORSAIR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V017000·2023-01-23
2022-2023 Isuzu N-Series and related commercial vehicles recalled for safety system miscalibration
Certain 2022-2023 Isuzu, Chevrolet, and Hino commercial vehicles with improperly calibrated ABS and optional ADAS camera systems are being recalled. The miscalibration could prevent the automatic emergency braking and electronic steering control systems from functioning properly, increasing crash risk.
Product
CHEVROLET — CHEVROLET, ISUZU, HINO LOW CAB FORWARD 5500, N-SERIES, S52
Category
Vehicle
Distribution
Distributed nationwide