NorthStar Arthritis Relief Cream Recalled for Microbial Contamination
Mariposa Labs is recalling NorthStar Arthritis Relief Cream because the product failed microbiological specifications.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall is classified as FDA Class II and involves microbial contamination, which presents a risk of harm even though specific injuries or illnesses are not reported in the source text.
Plain-English summary
Mariposa Labs, LLC is recalling 14,664 tubes of NorthStar Arthritis Relief Cream. The product is an over-the-counter cream in 2 oz tubes, manufactured for and distributed by NewMarket Health Products, LLC in Baltimore, Maryland.
The recall was initiated because the Arthritis Relief Cream failed microbiological specifications, indicating microbial contamination of the non-sterile product. The affected units are identified by the code 0106072/2298.
The recalled product was distributed to one consignee, who in turn sent it to one other consignee. Consumers should stop using the product and contact the recalling firm for instructions on disposal or return.
The recalled product
- 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
- Manufacturer
- Mariposa Labs, LLC
- Category
- Drug — Topical OTC
- Hazard
- Affected units
- 14,664
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- 0106072/2298
Distribution
Distribution scope not specified by the agency.
Related recalls
Same manufacturer · Mariposa Labs, LLC
See all →- ModerateTubby Todd Bath Co Dream Cream Recalled for Mold Contamination
FDA (Drugs) · 2019-02-27
Same hazard · microbial contamination
See all →- CriticalVictory Medical Center Pharmacy Recalls Glutathione Vials Due to Contamination
FDA (Drugs) · 2026-08-19
- HighMedline Medical Convenience Kits Recalled Due to Potential Bacillus Contamination
FDA (Devices) · 2026-07-29
- HighMedline Convenience Kits Recalled Over Bacillus Contamination
FDA (Devices) · 2026-07-29
- HighROHTO Cooling Eye Drops Recalled Over Sterility Assurance Concerns
FDA (Drugs) · 2026-07-29
- SeverePemetrexed for Injection Recalled Due to Lack of Sterility Assurance
FDA (Drugs) · 2026-07-15