Unrated Drug recall · FDA · Published August 24, 2021

Efficient Laboratories recalls Rompe Pecho Max bottles due to microbial contamination

Efficient Laboratories recalls Rompe Pecho Max Multi-Symptoms Maximum Strength bottles (8 fl oz) with microbial contamination risk. Consumers should check product details and contact the company for guidance.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0293-2022Drug Efficient Laboratories ›

Recall notice

Microbial Contamination of Non-Sterile Products

Take action

Contact the company

Recalling firmEfficient Laboratories, Inc.7715 NW 64th St · Miami, FL 33166-2719

✎ GovInfoNow plain-language explainer

Efficient Laboratories is recalling Rompe Pecho Max Multi-Symptoms Maximum Strength bottles (8 fl oz) because they may contain harmful microorganisms. This could lead to illness if the product is consumed. Read more at govinfonow.com/recall/35882-efficient-laboratories-recalls-rompe-pecho-max-bottles-due-to-microbial.

Source Summary by GovInfoNow · govinfonow.com/recall/35882-efficient-laboratories-recalls-rompe-pecho-max-bottles-due-to-microbial · Updated August 18, 2026 · FDA enforcement record: FDA #D-0293-2022

Cite this page

“Efficient Laboratories recalls Rompe Pecho Max bottles due to microbial contamination.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35882-efficient-laboratories-recalls-rompe-pecho-max-bottles-due-to-microbial. Based on FDA recall #D-0293-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0293-2022%22&limit=1).

The FDA announced on August 24, 2021, that Efficient Laboratories, Inc. is recalling Rompe Pecho Max Multi-Symptoms Maximum Strength bottles due to microbial contamination of non-sterile products. Owners should contact the company for a refund.

How to tell if you have it

Rompe Pecho Max Multi-Symptoms Maximum Strength, 8 Fl. Oz. (237 mL) bottles
UPC: 0 00856 00309 5
NDC: 58593-828-08
Lot #: 19G219
Expiration: July 2022

The hazard

The product poses a risk of microbial contamination because it is a non-sterile product. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show Efficient Laboratories, Inc. has one other recall on record since January 31, 2020. Other recent recalls of similar products include SV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination (September 1, 2026), Victory Medical Center Pharmacy Glutathione Vials Recall: Bacterial Contamination Risk (July 1, 2026), and Zep Alcohol Sanitizer Spray Recall: Microbial Contamination Risk (May 22, 2026).

How to tell if you have this one

Check for the product name 'Rompe Pecho Max Multi-Symptoms Maximum Strength', 8 fl oz (237 mL) bottles, and the lot number 19G219 with expiration date July 2022. The product was distributed by Efficient Laboratories, Inc. in Miami, FL.

Brand
Efficient Laboratories
Product
Rompe Pecho Max Multi-Symptoms Maximum Strength, 8 Fl. Oz. (237 mL) bottles, Distributed by: Efficient Laboratories
Category
Drug

FDA recall event · 4 products

All 4 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
Nationwide within the United States

Recall number	Product, codes & lots	Quantity	NDC
D-0290-2022	Rompe Pecho CF Cold & Flu Advanced Formula, 6 Fl. oz. (178 mL) bottles, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166, NDC 58593-235-06; Lot #: 19F88 Exp. June 2022; 19G164 Exp. July 2022.	10,833 bottles	58593-235-06, 58593-235-04, 58593-235-08, 58593-235-29, 58593-235-10
D-0291-2022	Rompe Pecho DM, 6 Fl Oz (178 mL) bottles, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166, NDC 58593-275-06; Lot #: 19F168 Exp. June 2022; 19G145, 19G361,19G449 19G491 Exp. July 2022.	27,206 bottles	58593-275-06, 58593-275-10, 58593-275-04, 58593-275-08
D-0292-2022	Rompe Pecho Ex Expectorant, packaged in a) 4 Fl. Oz. (118 mL) bottles NDC 58593-829-04 and b) 6 Fl. Oz. (178 mL) bottles NDC 58593-829-06, Distributed by Efficient Laboratories, Inc. Miami, FL 33166; Lot #: a) 19H20 Exp. August 2022; 19A418 Exp. January 2022; 19E411 Exp. May 2022; b) 19H20 Exp. August 2022; 19J98 Exp. September 2022; 19A418 Exp. January 2022; 19E411 Exp. May 2022	a) 7,800 bottles; b) 16,417 bottles	58593-829-06, 58593-829-04
D-0293-2022	Rompe Pecho Max Multi-Symptoms Maximum Strength, 8 Fl. Oz. (237 mL) bottles, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166 UPC 0 00856 00309 5, NDC 58593-828-08; Lot #: 19G219 Exp. July 2022	4,026 bottles	58593-828-08

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the product name, size, lot number, and expiration date on the bottle label.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Nationwide within the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 15 months after the firm started it.

Aug 24, 2021Firm started the recall
Dec 22, 2021FDA classified it Class II
Dec 29, 2021Published in FDA’s Enforcement Report
Dec 8, 2022FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

Is this product safe to use?

The recall indicates a potential microbial contamination risk, so it is not safe to use. Consumers should check the product details and follow the action steps.

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Link to this recall

<a href="https://govinfonow.com/recall/35882-efficient-laboratories-recalls-rompe-pecho-max-bottles-due-to-microbial">Efficient Laboratories recalls Rompe Pecho Max bottles due to microbial contamination (GovInfoNow)</a>

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-0293-2022 (August 24, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0293-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.