FDA Drugs recall ·
Rheumacare capsules, 30 count bottle, Mfg in India by: Virgo UAP Pharma Pvt recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0332-2026
- Date
- (initiated December 22, 2025)
- Company / brand
- Handelnine Global LLC
South Plainfield, South Plainfield, NJ, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 4 bottles /30 capsules each
- Hazard tags
- Lead Manufacturing practices (cGMP)
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Rheumacare capsules, 30 count bottle, Mfg in India by: Virgo UAP Pharma Pvt. Ltd., Ahmedabad, India UPC 8 904218 700313
Why was it recalled?
CGMP Deviations: product found to contain lead.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot: CAM040, Exp. 06/30/2029 Lot: CAL079-N, Exp. 09/30/2028
Distribution
Product was distributed to one customer in NY.
States: New York
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0332-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.