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Class II: temporary or reversible health riskTerminated

Mariposa Labs NorthStar Arthritis Relief Cream Recall

NorthStar Arthritis Relief Cream

Mariposa Labs, LLC · Boise, ID

Risk level
Class II
Reported by FDA
Jan 22, 2014
Recall ID
D-462-2014
Check your lot numberHow we source this data

Summary

Mariposa Labs recalled NorthStar Arthritis Relief Cream starting Nov 29, 2012. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-462-2014 on Jan 22, 2014. Reason: Microbial Contamination of Non-Sterile Products: Arthritis Relief Cream failed microbiological specifications. Status: Terminated.

Why it was recalled

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

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

Lot numbers, UPCs & expiration codes

0106072/2298

Where it was sold

One consignee who in turn sent it to one consignee

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-462-2014
Classification
Class II
Status
Terminated
Recall initiated
Nov 29, 2012
FDA report date
Jan 22, 2014
Quantity
14,664 tubes
Recall type
Voluntary: Firm initiated
Recalling firm
Mariposa Labs, LLC

Original FDA data

Every field from FDA enforcement report D-462-2014, exactly as published.

Show all FDA fields
City
Boise
State
ID
Status
Terminated
Country
United States
Event ID
67088
Address
270 E 50th St
Code information
0106072/2298
Postal code
83714-1428
Report date
Jan 22, 2014
Product type
Drugs
Recall number
D-462-2014
Classification
Class II
Recalling firm
Mariposa Labs, LLC
Product quantity
14,664 tubes
Termination date
Jan 17, 2014
Reason for recall
Microbial Contamination of Non-Sterile Products: Arthritis Relief Cream failed microbiological specifications.
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
One consignee who in turn sent it to one consignee
Recall initiation date
Nov 29, 2012
Initial firm notification
E-Mail
Center classification date
Jan 14, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-462-2014, published Jan 22, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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