ProSupps USA recalls 8oz Green Apple flavor pre-workout supplement due to exceeding declared yohimbine HCL levels. Consumers should check UPC 682055405483 and lot numbers 0116L1/0117L1 for affected products.
The product contains more yohimbine hcl than declared on the label
ProSupps USA is recalling their Intense Energy Pre Workout supplement because it contains more yohimbine HCL than labeled. This could pose health risks if consumed, though the exact danger isn: not specified in the recall.
The product contains more yohimbine HCL than declared on the label. Yohimbine HCL is a stimulant that can cause increased heart rate, blood pressure, and anxiety if taken in excess. However, the recall does not specify how much excess is present or the exact health risks.
People who purchased the Green Apple flavored pre-workout supplement with UPC 682055405483 and lot numbers 0116L1 or 0117L1 are affected. Those using this supplement for energy or athletic performance may be at higher risk.
Check for the product name 'MR. HYDE INTENSE ENERGY PRE WORKOUT', Green Apple flavor, 8.0 oz size, and UPC 682055405483 with lot numbers 0116L1 or 0117L1.
Identify the product by checking the UPC 682055405483 and lot numbers 0116L1 or 0117L1.
The recall states the product contains more yohimbine HCL than declared, but does not specify the exact health risks or how much excess is present.
Look for the product name 'MR. HYDE INTENSE ENERGY PRE WORKOUT', Green Apple flavor, 8.0 oz size, UPC 682055405483 with lot numbers 0116L1 or 0117L1.
The recall does not provide a specific remedy, so the official notice does not state what action to take.
We’ve drafted a message you can send ProSupps to request your refund or repair — edit it as you like.
Subject: Recall F-1783-2015 — ProSupps ProSupps Hello, I own a ProSupps that is covered by recall F-1783-2015 from ProSupps. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
