PlainRecalls
FDA Drug Moderate Class II Terminated

Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-858-01

Reported: March 18, 2020 Initiated: March 2, 2020 #D-0998-2020

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.

Details

Recalling Firm
Mayne Pharma Inc
Units Affected
8274 100-count bottles
Distribution
Distributed Nationwide in the USA
Location
Greenville, NC

Frequently Asked Questions

What product was recalled?
Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-858-01. Recalled by Mayne Pharma Inc. Units affected: 8274 100-count bottles.
Why was this product recalled?
Product Mix-Up: A foreign tablet was found in bottle.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 18, 2020. Severity: Moderate. Recall number: D-0998-2020.