Rompe Pecho MAX Recall: Microbial Contamination Risk
Efficient Laboratories recalls New! Rompe Pecho MAX due to microbial contamination. Check lot 19B42, exp Feb 2022.
Use caution until it’s fixed
Microbial Contamination of Non-Sterile Products
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What happened, in plain English
Efficient Laboratories, Inc. is recalling New! Rompe Pecho MAX Multi Symptoms because the non-sterile product may be contaminated with microorganisms. The recall covers 4,080 bottles distributed nationwide in the USA. No specific remedy or consumer action steps are currently listed in the record. Read more at govinfonow.com/recall/37387-rompe-pecho-max-recall-microbial-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37387-rompe-pecho-max-recall-microbial-contamination-risk · Updated October 11, 2026 · FDA enforcement record: FDA #D-0847-2020
Cite this page
“Rompe Pecho MAX Recall: Microbial Contamination Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/37387-rompe-pecho-max-recall-microbial-contamination-risk. Based on FDA recall #D-0847-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0847-2020%22&limit=1).
Why it’s dangerous
The product is classified as non-sterile, meaning it was not manufactured under conditions that guarantee freedom from microorganisms. If the product contains harmful microbes, using it could lead to infection or other health issues, particularly for those with compromised immune systems.
Who’s affected
Consumers who purchased New! Rompe Pecho MAX Multi Symptoms from retailers across the United States between distribution and January 31, 2020. Individuals using this specific chest pain relief supplement are at risk of exposure to microbial contamination.
How to tell if you have this one
Check your bottle for the brand name "New! Rompe Pecho MAX Multi Symptoms" and a size of 8 FL. Oz (237 mL). Verify if the UPC is 0 00856 00309 5, the Lot number is 19B42, and the expiration date is February 2022.
- Brand
Efficient Laboratories- Product
New! Rompe Pecho MAX Multi Symptoms, 8 FL. Oz (237 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL- Category
Drug
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Distributed Nationwide in the USA
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0845-2020 | Rompe Pecho CF Cold & Flu with Honey, 6 FL. Oz (178 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166.UPC 0 00856 33106 8; Lot: 19H359 Exp. August 2022 | 5249 6 Fl Oz bottles |
| D-0846-2020 | Rompe Pecho EX Expectorant, 6 FL. Oz (178 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166. UPC 0 00856 30106 1; Lot: 19F332 Exp. June 2022 | 5387 6 Fl Oz bottles |
| D-0847-2020 | New! Rompe Pecho MAX Multi Symptoms, 8 FL. Oz (237 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166. UPC 0 00856 00309 5; Lot: 19B42 Exp. February 2022 | 4080 8 FL Oz bottles |
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Distributed Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
How many units are being recalled?
Approximately 4,080 bottles of 8 FL. Oz size are included in this recall.
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Where this comes from
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.
- Official source: FDA Recall #D-0847-2020 (January 31, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0847-2020 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.