HIGH

HANDELNINE GLOBAL Recalls Rheumacare Capsules Due to Lead Risk

HANDELNINE GLOBAL recalled Rheumacare capsules on December 22, 2025, after discovering lead contamination. The recall affects four bottles of 30 capsules each distributed in New York. Consumers should stop using the product immediately and contact their healthcare provider.

Quick Facts at a Glance

Recall Date
December 22, 2025
Hazard Level
HIGH
Brand
HANDELNINE GLOBAL
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

CGMP Deviations: product found to contain lead.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact HANDELNINE GLOBAL LLC or your healthcare provider for guidance. Notification method: Press Release

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Product Details

The recall involves Rheumacare capsules, sold in 30-count bottles. The affected lots include CAM040, CAL079-N (exp. 06/30/2029), and another with an expiration of 09/30/2028.

The Hazard

The product contains lead, posing serious health risks if ingested. Lead exposure can result in severe health issues, particularly affecting the nervous system.

Reported Incidents

There have been no specific incidents or injuries reported in connection with this product. However, the presence of lead raises significant health concerns.

What to Do

Stop using the Rheumacare capsules immediately. Contact HANDELNINE GLOBAL LLC or your healthcare provider for further guidance.

Contact Information

For more information, visit the FDA website or contact HANDELNINE GLOBAL LLC directly. The recall notice is available at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0332-2026.

Key Facts

  • Recalled on December 22, 2025
  • Contains lead, a hazardous substance
  • Distributed to one customer in New York
  • No reported injuries or incidents

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
POISONING

Product Details

Model Numbers
Lot: CAM040
Exp. 06/30/2029 Lot: CAL079-N
Exp. 09/30/2028
Affected States
NY
Report Date
February 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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