FDANovember 3, 2025device
DHEA Test
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Distribution without premarket approval/clearance.
What to do
FDA enforcement status: Ongoing
Brands named
get tested international abgetget tested
UPCs
616612786418
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- CPSCSUNS International Recalls Residential Elevator Interlock Switches Due to Fall and Crushing Hazard; Risk of Death or Serious Injury2026-06-04
- FDADairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, 50 lb bags2026-05-18
- FDADairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box2026-05-18
- FDALegacy Tex Dressing Stabilizer Blend #7604-50, 50lb bags2026-05-18
- FDAVitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400 bottle, 47 SERVING PER BOTTLE, 24 bottles- 8 FL Oz (237mL) Amber PET modern round bottles per package, Store at room. Mnfg by: Llorens Pharmaceutical Miami, FL2026-05-07
- CPSCVitaquest International Recalls Multiple Iron Supplement Bottles and Packets Due to Risk of Serious Injury or Death from Poisoning to Young Children; Violates Mandatory Standard for Child-Resistant Packaging2026-04-09
- CPSCSamson International Recalls Bellevue and Oaklynn Canopy Bed Frames Due to Impact and Injury Hazards2026-04-02
- FDAEPINEPHRINE Injection, USP, 1 mg/10mL (0.1 mg/mL), Rx only, INTERNATIONAL MEDICATION SYSTEMS, LIMITED, So. EL Monte, CA 91733, An Amphastar Pharmaceutical Company, NDC 76329-3318-12026-04-01
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