FindMyRecallSubscribe
Class I: serious health riskOngoing

Handelnine Global Rheumacare capsules Recall

Rheumacare capsules, 30 count bottle, Mfg in India by: Virgo UAP Pharma Pvt

HANDELNINE GLOBAL LLC · South Plainfield, NJ

Risk level
Class I
Reported by FDA
Feb 11, 2026
Recall ID
D-0332-2026
Check your lot numberHow we source this data

Summary

Handelnine Global recalled Rheumacare capsules starting Dec 22, 2025. The FDA classified it as Class I (serious health risk) and published enforcement report D-0332-2026 on Feb 11, 2026. Reason: CGMP Deviations: product found to contain lead. Status: Ongoing.

Why it was recalled

CGMP Deviations: product found to contain lead.

Product description

Rheumacare capsules, 30 count bottle, Mfg in India by: Virgo UAP Pharma Pvt. Ltd., Ahmedabad, India UPC 8 904218 700313

Lot numbers, UPCs & expiration codes

Lot: CAM040, Exp. 06/30/2029 Lot: CAL079-N, Exp. 09/30/2028

Where it was sold

Product was distributed to one customer in NY.

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-0332-2026
Classification
Class I
Status
Ongoing
Recall initiated
Dec 22, 2025
FDA report date
Feb 11, 2026
Quantity
4 bottles /30 capsules each
Recall type
Voluntary: Firm initiated
Recalling firm
HANDELNINE GLOBAL LLC

Original FDA data

Every field from FDA enforcement report D-0332-2026, exactly as published.

Show all FDA fields
City
South Plainfield
State
NJ
Status
Ongoing
Country
United States
Event ID
98165
Address
South Plainfield
Address (line 2)
4300 S Clinton Ave
Code information
Lot: CAM040, Exp. 06/30/2029 Lot: CAL079-N, Exp. 09/30/2028
Postal code
07080-1219
Report date
Feb 11, 2026
Product type
Drugs
Recall number
D-0332-2026
Classification
Class I
Recalling firm
HANDELNINE GLOBAL LLC
Product quantity
4 bottles /30 capsules each
Reason for recall
CGMP Deviations: product found to contain lead.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Rheumacare capsules, 30 count bottle, Mfg in India by: Virgo UAP Pharma Pvt. Ltd., Ahmedabad, India UPC 8 904218 700313
Distribution pattern
Product was distributed to one customer in NY.
Recall initiation date
Dec 22, 2025
Initial firm notification
Press Release
Center classification date
Feb 12, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0332-2026, published Feb 11, 2026. 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.

How we source and update recall data · Report incorrect information

Other recent drug recalls