February 2016 FDA Recall Drug by Keystone Laboratories Inc
D-0726-2016 - Microbial Contamination of a Non-Sterile Products
This Class II drug recall was voluntarily initiated by Keystone Laboratories Inc on February 8, 2016 for the product Drug. The FDA reported the reason for recall as microbial contamination of a non-sterile products. The product was distributed Nationwide and the recall is currently terminated.
Recall Number: D-0726-2016
Microbial Contamination of a Non-Sterile Products: The product had a positive Staphylococcus aureus test result.
02-08-2016
03-02-2016
134 cases of 12 bottles/case
Recall Profile & Regulatory Data
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
The firm responsible for the recall.
Keystone Laboratories Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Method by which the firm first notified the public.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
General area of initial distribution.
Nationwide and Canada
05-25-2016
Product Description About Product Description
Full technical description of the product.
Full technical description of the product.
Medicated Better Braids, La Laque (salicylic acid) Spray, 2%,12 Fl. OZ. (355 ml.) bottle, Distributed by Keystone Laboratories, Memphis, TN 38101-2026, UPC 0 70596 00422 5.
Batch or Lot Expiration Information
Lot# : 9AD5