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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

About This Product

Rheumacare capsules are marketed as dietary supplements for joint pain relief. Consumers often buy them for managing arthritis and other inflammatory conditions.

Why This Is Dangerous

The presence of lead in the capsules presents a significant health risk. Lead is a toxic metal that can cause serious health issues, particularly affecting the nervous system and various bodily functions.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers are advised to stop using the product immediately, as lead ingestion can lead to severe health complications. Financial impacts may include the cost of alternative treatments and potential medical expenses.

Practical Guidance

How to identify if yours is affected

  1. Check the lot number on the bottle: CAM040, CAL079-N, or the expiration date of 09/30/2028.
  2. If your lot number matches, stop using the product immediately.
  3. Contact the distributor for further guidance.

Where to find product info

The lot number and expiration date can typically be found on the label or bottom of the bottle.

What timeline to expect

Expect a refund or guidance within 4-6 weeks after contacting the distributor.

If the manufacturer is unresponsive

  • Document all communication attempts with the distributor.
  • Consider filing a complaint with the FDA if no response is received.

How to prevent similar issues

  • Always check for recalls before purchasing dietary supplements.
  • Look for products with verified safety certifications.

Documentation advice

Keep a record of your purchase, including receipts and any correspondence with the distributor.

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.

Key Facts

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

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

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

Related Recalls

Health & Personal Care
MEDIUM

AvKARE Recalls Rosuvastatin Tablets Due to Dissolution Issues

AvKARE recalled 7,991 cartons of Rosuvastatin Tablets on December 31, 2025. The recall stems from the product being out of specification for dissolution. Consumers should stop using the medication immediately and consult healthcare providers for guidance.

LACTATED RINGERS
Presence of
Read more
Recalled ZOLIQUEX Bed Rail (front view)
HIGH

ZOLIQUEX Adult Portable Bed Rails Recalled for Entrapment, Asphyxiation Risk (2026)

ZOLIQUEX recalled adult portable bed rails sold on Amazon after reports of entrapment and asphyxiation risk. The recall targets silver bed rails measuring 12.4 inches wide by 33.07 inches tall and weighing 7.1 pounds. The model numbers ZEX014-V1 and the Zoliquex branding appear on packaging. Stop using the product and seek a full refund by contacting ZOLIQUEX.

ZOLIQUEX, of China
The recalled
Read more
Recalled Arey, Not Today, Grey (180ct) - front
HIGH

Vitaquest International Recalls Multiple Iron Supplements for Child-Resistant Packaging Violations (

Vitaquest International recalled Arey Not Today iron supplements sold at retailers nationwide after determining the products do not meet the Poison Prevention Packaging Act's child-resistant packaging requirement. The noncompliant packaging creates a poisoning risk to young children if ingested. Consumers should stop using the products immediately and contact Vitaquest for a free child-resistant替换

Vitaquest International LLC of West Caldwell, New Jersey
The dietary
Read more
Recalled Easymake Bed Rail
HIGH

Easymake Adult Portable Bed Rails Recalled for Entrapment Risk (2026)

Easymake adult portable bed rails imported by ZFZG-US are recalled on April 9, 2026. The recall cites a risk of entrapment and asphyxiation and notes the product lacks required hazard warning labels. Stop using the recalled rails immediately and contact ZFZG-US for a full refund.

Zhongshan Yungu Daily Products, of China
The recalled
Read more
Recalled Tuymec Minoxidil Hair Growth Serum Spray Bottle (front and back)
HIGH

Tuymec Minoxidil Hair Growth Kit Recalled for Non-Child-Resistant Packaging (2026)

Tuymec Minoxidil Hair Growth Kit sold on Amazon by DrHealBeauty is recalled for non-child-resistant packaging. The kit contains two black spray bottles with 5% minoxidil and BIOTIN labels. Consumers should stop using the product immediately and contact DrHealBeauty for a free empty replacement bottle with a child-resistant closure.

Tuymec Minoxidil Hair Growth Spray Bottles
The hair
Read more
Recalled TecFlox Topical Solution - hair and beard growth serum bottle
HIGH

TecFlox Minoxidil Topical Solution Hair Serum Recalled for Child Poisoning Risk (2026)

TecFlox recalled its Minoxidil Topical Solution hair growth serum bottles on April 2, 2026. The packaging is not child-resistant, violating the Poison Prevention Packaging Act. Consumers should stop using the product immediately, store it out of reach of children, and email TecFloxrecall@outlook.com to receive free replacement bottles. Only bottles with serum remaining will be replaced; dispose of

TecFlox Hair and Beard Growth Serum Bottles
The hair
Read more