Bruder Thermalon Sinus Compress Recall: Mold Risk from Moisture Exposure

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Recalling firmBruder Healthcare Company, LLC1115 Ridgeland Pkwy Ste 101, N/A · Alpharetta, GA 30004-8409

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Bruder Healthcare is recalling Thermalon Sinus Compresses from certain lots because they may have been exposed to excessive moisture, which could lead to mold or mildew growth. This poses a health risk if the compresses are used without proper drying.

Why it’s dangerous

The compresses may have been exposed to excessive moisture during manufacturing, creating conditions where mold and mildew can grow. If used without proper drying, these growths could cause health issues like allergic reactions or infections.

Who’s affected

People who own or use Thermalon Sinus Compresses (Item : 24332) from specific lots are affected. Those with compromised immune systems may be at higher risk from mold exposure.

How to tell if you have this one

Check for the item number 24332 on the compress packaging. Affected lots are M053160 and M053570. The UPC code is 041533243328.

Brand
Bruder Healthcare
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for lot numbers M053160 or M053570 on the Thermalon Sinus Compress packaging.
Discard Affected Units
If you have the affected lot numbers, discard the compresses to avoid potential mold or mildew growth.

✎ GovInfoNow

Questions people ask

What lot numbers are affected?

Lot numbers M053160 and M053570 are affected.

How can I tell if I have the recalled product?

Check the item number 24332 on the packaging and look for lot numbers M053160 or M053570.

Do I need to do anything if I have the product?

If you have the affected lot numbers, discard the compresses to avoid potential mold or mildew growth.

Take action

Contact Bruder Healthcare

We’ve drafted a message you can send Bruder Healthcare to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1361-2024 — Bruder Healthcare Bruder Healthcare

Hello,

I own a Bruder Healthcare that is covered by recall Z-1361-2024 from Bruder Healthcare.

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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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 #Z-1361-2024 (February 21, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1361-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.

Bruder Healthcare Company, LLC recalls Thermalon Sinus Compress, Item Number 24332

Lower-risk recall