Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville...
FDA Recall #D-0998-2020 — Class II — March 2, 2020
Product Description
Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-858-01
Reason for Recall
Product Mix-Up: A foreign tablet was found in bottle.
Recalling Firm
Mayne Pharma Inc — Greenville, NC
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Drugs
Product Quantity
8274 100-count bottles
Distribution
Distributed Nationwide in the USA
Code Information
Lot: FG11514 Exp. 05/2021
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated
What Should You Do?
Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.