GM Manufacturing recalls BTI Lean Formula dietary supplements in 400cc HDPE bottles due to significant cGMP regulatory violations. Consumers should check product labels for the model number LT7345 EX10.16.
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
GM Manufacturing is recalling BTI Lean Formula dietary supplements in 40:00cc HDPE bottles because they violated food safety regulations. This recall is due to significant violations of cGMP rules, which could affect product safety.
The product was recalled because GM Manufacturing violated cGMP regulations for dietary supplements. These violations could lead to unsafe product quality, but the specific hazard mechanism is not clearly described in the recall notice.
Dietary supplement users who own the BTI Lean Formula 400cc HDPE bottles with model number LT7345 EX10.16 are affected. Those who have consumed the product may be at risk due to regulatory violations.
Check for the model number LT7345 EX10.16 on the bottle label. The product is a 400cc HDPE bottle of BTI Lean Formula dietary supplement.
Look for the model number LT7345 EX10.16 on the bottle label to confirm if the product is recalled.
GM Manufacturing is recalling these dietary supplements due to significant violations of cGMP regulations for dietary supplements.
The recall notice does not specify a remedy, so check the product label for the model number LT7345 EX10.16 to confirm if it's affected.
The recall notice does not describe a specific hazard mechanism, so the risk level is unknown.
We’ve drafted a message you can send GM Manufacturing to request your refund or repair — edit it as you like.
Subject: Recall F-2265-2014 — GM Manufacturing GM Manufacturing Hello, I own a GM Manufacturing that is covered by recall F-2265-2014 from GM Manufacturing. 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.
