FDA-Drug2014-01-22Class II

PRAMIPEXOLE DI-HCL Tablet, 0.25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714058501

Aidapak Services, LLC
Hazard

Labeling: Label Mixup; PRAMIPEXOLE DI-HCL, Tablet, 0.25 mg may be potentially mislabeled as TACROLIMUS, Capsule, 1 mg, NDC 00781210301, Pedigree: W003704, EXP: 6/26/2014.

Sold states
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Affected count
90 Tablets
Manufactured in
14301 Se 1st St, Vancouver, WA, United States
Products
PRAMIPEXOLE DI-HCL Tablet, 0.25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714058501

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-521-2014

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief