February 2016 FDA Recall Drug by J. Strickland And Co
D-0734-2016 - Subpotent Drug

This Class III drug recall was voluntarily initiated by J. Strickland And Co on February 11, 2016 for the product Drug. The FDA reported the reason for recall as subpotent drug. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0734-2016

Reason for Recall
Subpotent Drug: failed at the 3 and 6 month stability time points.
Initiated
02-11-2016
Reported
03-09-2016
Quantity
1170 cases

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
73332
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class III - is a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
J. Strickland and Co
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide, Jamaica and Bahamas
Termination Date About Termination Date
Date that FDA officially terminated the recall.
11-22-2016
Product Description About Product Description
Full technical description of the product.
sulfur8 medicated LIGHT FORMULA (sulfur) anti-dandruff hair & scalp conditioner, 2%, packaged in a) 2 OZ (57g) jar (UPC 0 75610 43510 8), and b) 4 OZ (113g) jar (UPC 0 75610 43610 5), 1 dozen jars per case, J. Strickland & Co., PO Box 1637, Olive Branch, MS 38654

Batch or Lot Expiration Information

Lot# : 33UF