AvKARE: Drug Recall

Recall #D-0460-2025 · 05/13/2025

Class II: Risk

Recall Details

Recall Number
D-0460-2025
Classification
Class II
Product Type
Drug
Recalling Firm
AvKARE
Status
Ongoing
Date Initiated
05/13/2025
Location
Pulaski, TN, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
3,817 50-count cartons

Reason for Recall

Presence of Foreign Tablets/Capsules: manufacturer recalled because one tadalafil 5mg tablet was found in 500 count bottle of Celecoxib 200 mg capsules

Product Description

Celecoxib Capsules, 200 mg, 50 Capsules (5x10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC 50268-169-15

Distribution Pattern

Nationwide in the USA

Other Recalls by AvKARE

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Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.