Marcas Usa Recalls Zinc Oxide Skin Cream Due to Microbial Contamination
Marcas Usa recalls 60g zinc oxide skin cream with microbial contamination risk. Products with lot numbers 15PL041-17LP117 and expiration dates up to 10/20 may be unsafe.
Lower-risk recall
Microbial Contamination of Non-Sterile Products
Contact the company
What happened, in plain English
Marcas Usa is recalling a zinc oxide skin cream product due to microbial contamination. This could cause skin infections if used. Consumers should stop using the product if they have the recalled items. Read more at govinfonow.com/recall/40708-marcas-usa-recalls-zinc-oxide-skin-cream-due-to-microbial.
Source Summary by GovInfoNow · govinfonow.com/recall/40708-marcas-usa-recalls-zinc-oxide-skin-cream-due-to-microbial · Updated October 7, 2026 · FDA enforcement record: FDA #D-0628-2018
Cite this page
“Marcas Usa Recalls Zinc Oxide Skin Cream Due to Microbial Contamination.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40708-marcas-usa-recalls-zinc-oxide-skin-cream-due-to-microbial. Based on FDA recall #D-0628-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0628-2018%22&limit=1).
Why it’s dangerous
The cream contains microbial contamination, which can lead to skin infections. This is a non-sterile product that may not be safe for direct skin contact.
Who’s affected
People who own or use the recalled zinc oxide skin cream product. Those with sensitive skin or open wounds may be at higher risk.
How to tell if you have this one
Check for the product name 'PASTA DE LASSAR ANDROMACO Skin Protection', 60g tube, UPC #851357003004, NDC #75940-111-60. Look for lot numbers 15PL041, 15PL040, 15PL039, or 17LP117 with expiration dates up to 10/20.
- Brand
Marcas Usa- Product
PASTA DE LASSAR ANDROMACO Skin Protection, 25% zinc oxide Topical cream, 60 gram tube, UPC #851357003004, NDC- Category
Drug
What to do — step by step
Check Product Details
Identify the product by checking the UPC #851357003004 and lot numbers listed in the recall notice.
Stop Using Product
Discontinue use of the recalled cream if you have the affected lot numbers.
Where it went and when
Where it was distributed
Distributed in Texas.
FDA distribution: “TX” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Texas.
Recall timeline
FDA terminated this recall 10 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.
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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-0628-2018 (March 30, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0628-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.