PlainRecalls
FDA Drug Moderate Class II Terminated

Phenobarbital/Hyoscyamine/ Atropine/Scopolamine 16.2/0.1037/0.0194/0.0065 mg DONNATAL ELIXIR, 5 ml Cup grape, Alcohol 23.8%, Rx Only, MFG: Concordia, PKG BY: SAFECOR HEALTH, WOBURN, MA, C5921242304.

Reported: April 6, 2016 Initiated: July 16, 2015 #D-0785-2016

Product Description

Phenobarbital/Hyoscyamine/ Atropine/Scopolamine 16.2/0.1037/0.0194/0.0065 mg DONNATAL ELIXIR, 5 ml Cup grape, Alcohol 23.8%, Rx Only, MFG: Concordia, PKG BY: SAFECOR HEALTH, WOBURN, MA, C5921242304.

Reason for Recall

Labeling: Label Error on Declared Strength: Label incorrectly identifies product dose as 5ml instead of 10 ml.

Details

Recalling Firm
Safecor Health, LLC
Units Affected
23 cups
Distribution
NY
Location
Woburn, MA

Frequently Asked Questions

What product was recalled?
Phenobarbital/Hyoscyamine/ Atropine/Scopolamine 16.2/0.1037/0.0194/0.0065 mg DONNATAL ELIXIR, 5 ml Cup grape, Alcohol 23.8%, Rx Only, MFG: Concordia, PKG BY: SAFECOR HEALTH, WOBURN, MA, C5921242304.. Recalled by Safecor Health, LLC. Units affected: 23 cups.
Why was this product recalled?
Labeling: Label Error on Declared Strength: Label incorrectly identifies product dose as 5ml instead of 10 ml.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 6, 2016. Severity: Moderate. Recall number: D-0785-2016.