GNMart Inc. is voluntarily recalling all lots of its Force Forever Joint Pain supplement, packaged in 60-tablet bottles with a white plastic container and a red cap, following an FDA analysis that found the product contains undeclared ingredients, Diclofenac and Dexamethasone.
The company’s recall involves all lots of the supplement, which is labeled as FORCE FOREVER with an expiration date of March 27, 2030. The affected product was marketed as a dietary supplement for joint pain and distributed nationwide through GNMart’s website at gnmart.com, and is being recalled to the consumer level.
Health Risks and Warnings
The inclusion of Diclofenac, a non-steroidal anti-inflammatory drug (NSAID), and Dexamethasone, a corticosteroid, pose serious health risks if consumed unknowingly.
Diclofenac has been associated with an increased risk of cardiovascular issues such as heart attacks and strokes, as well as severe gastrointestinal problems, including bleeding, ulcers, and even fatal stomach or intestinal perforation.
Dexamethasone, commonly prescribed for inflammatory conditions, can weaken the immune system, increase blood sugar levels, and lead to muscle injuries or psychiatric issues, including mood swings and depression. Given these risks, GNMart advises all consumers to stop using the product immediately and return it to the place of purchase.
GNMart Inc. has stated that, as of now, the company has not received any reports of adverse health events linked to the use of the product. However, the company is urging consumers to contact their healthcare providers if they have experienced any issues related to the supplement.
Customers who have purchased the recalled “Force Forever” Joint Pain supplement should immediately cease use and return the product to GNMart. The company is notifying customers by email and arranging for the return of all recalled items. Consumers can return the product via mail to the following address:
GNMart, Inc.
15 Sawmill Ln
Dover Plains, NY 12522
Consumers with questions can contact GNMart via email at [email protected]. Customer support is available Monday through Friday from 9 a.m. to 5 p.m. EST, with a response time of 24 to 48 hours.
Reporting Adverse Events
Anyone who has experienced adverse reactions or quality issues with the recalled product is encouraged to report these incidents to the FDA’s MedWatch Adverse Event Reporting program. Reports can be made online, by regular mail, or by fax.
For more information, consumers are advised to stay updated through official channels from GNMart and the FDA.