Efficient Laboratories recalls Rompe Pecho CF Cold & Flu Advanced Formula bottles with microbial contamination risk. Consumers should check lot numbers and contact the company for details.
Microbial Contamination of Non-Sterile Products
Efficient Laboratories is recalling Rompe Pecho CF Cold & Flu Advanced Formula bottles that may contain microbial contamination. This could pose a health risk if consumed, so affected consumers should stop using the product.
Microbial contamination in non-sterile products can lead to infections or illnesses if the product is consumed. This is a serious health hazard because the product is intended for consumption and not meant to be sterile.
Anyone who owns or uses Rompe Pecho CF Cold & Flu Advanced Formula bottles with lot numbers 19F88 (expiring June 2022) or 19G164 (expiring July 2022) is affected. Children and elderly individuals may be at higher risk due to potential health impacts.
Check the lot number on the bottle, which is either 19F88 (expiring June 2022) or 19G164 (expiring July 2022). The product is distributed by Efficient Laboratories, Inc. in Miami, Florida.
Immediately stop using the recalled Rompe Pecho CF Cold & Flu Advanced Formula bottles with lot numbers 19F88 or 19G164.
The recalled bottles have lot numbers 19F88 (expiring June 2022) or 19G164 (expiring July 2022).
Check the lot number on the bottle, which should be either 19F88 (expiring June 2022) or 19G164 (expiring July 2022).
Immediately stop using the product and contact Efficient Laboratories, Inc. for further instructions.
We’ve drafted a message you can send Efficient Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0290-2022 — Efficient Laboratories Efficient Laboratories Hello, I own a Efficient Laboratories that is covered by recall D-0290-2022 from Efficient Laboratories. 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.
