November 2012 FDA Recall Drug by Mariposa Labs, Llc
D-462-2014 - Microbial Contamination of Non-Sterile Products
This Class II drug recall was voluntarily initiated by Mariposa Labs, Llc on November 29, 2012 for the product Drug. The FDA reported the reason for recall as microbial contamination of non-sterile products. The product was distributed in One consignee who in turn sent it to one consignee and the recall is currently terminated.
Recall Number: D-462-2014
Microbial Contamination of Non-Sterile Products: Arthritis Relief Cream failed microbiological specifications.
11-29-2012
01-22-2014
14,664 tubes
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.
Mariposa Labs, LLC
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.
E-Mail
Distribution Pattern About Distribution Pattern
General area of initial distribution.
General area of initial distribution.
One consignee who in turn sent it to one consignee
01-17-2014
Product Description About Product Description
Full technical description of the product.
Full technical description of the product.
NorthStar Arthritis Relief Cream. Net Wt. 2 oz tube, OTC, Manufactured for and Distributed by NewMarket Health Products, LLC. 702 Cathedral St. Baltimore, MD 21201
Batch or Lot Expiration Information
Lot# 0106072/2298
