FDA recall record

Mariposa Labs NorthStar Arthritis Relief Cream recall — FDA D-462-2014

Microbial Contamination of Non-Sterile Products: Arthritis Relief Cream failed microbiological specifications.

Class IIclassification
D-462-2014official record ID
Jan 22, 2014report date

Recall record at a glance

Official recordD-462-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMariposa Labs, LLC
Report dateJan 22, 2014
Recall initiation dateNov 29, 2012
Quantity14,664 tubes
LocationBoise, ID, United States

Official product description

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

Why the product was recalled

Microbial Contamination of Non-Sterile Products: Arthritis Relief Cream failed microbiological specifications.

Distribution information

One consignee who in turn sent it to one consignee

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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