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Lower risk Medical device recall · FDA · Published November 18, 2019

Southwest Technologies Elasto-Gel Wound Dressings Recalled Due to Mold Contamination Risk

Southwest Technologies recalls 5 sterile Elasto-Gel wound dressings (4" x 4") with UPC 45713-58000 that may be contaminated with mold. Consumers should check lot numbers and contact the company for details.

🇺🇸 FDA recall #Z-0687-2020Medical deviceSouthwest Technologies ›
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Contact the company

Recalling firmSouthwest Technologies Inc1746 E Levee St · Kansas City, MO 64116-4404
✎ GovInfoNow plain-language explainer

Southwest Technologies is recalling 5 sterile Elasto-Gel wound dressings (4" x 4") that may be contaminated with mold. Using these dressings could lead to infection or other health issues if mold is present. Read more at govinfonow.com/recall/66513-southwest-technologies-elasto-gel-wound-dressings-recalled-due-to-mold.

Source Summary by GovInfoNow · govinfonow.com/recall/66513-southwest-technologies-elasto-gel-wound-dressings-recalled-due-to-mold · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0687-2020

Cite this page

“Southwest Technologies Elasto-Gel Wound Dressings Recalled Due to Mold Contamination Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/66513-southwest-technologies-elasto-gel-wound-dressings-recalled-due-to-mold. Based on FDA recall #Z-0687-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0687-2020%22&limit=1).

The FDA announced on November 18, 2019, that Southwest Technologies Inc voluntarily recalled Elasto-Gel Absorbent Wound Dressing due to potential mold contamination. The recall affects approximately 3,260 units distributed in California, Georgia, Illinois, Kansas, New York, Ohio, Tennessee, Texas, and Virginia.

How to tell if you have it

  • Brand: Southwest Technologies
  • Product: Elasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Sterile. UPC 45713-58000 Bacteriostatic
  • Lot code: 1917802
  • UPC: 4571358000

The hazard

The Elasto-Gel Wound Dressing may be contaminated with mold. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show Southwest Technologies Inc has two other recalls on record since December 28, 2017. On May 28, 2021, the company recalled Stimulen Lotion due to dose audit failure risk after sterilization. Other recent recalls of similar products include Medline Sterile Saline Wound Wash Recall (January 5, 2026), Integra CVS Wound Dressing Recall (January 16, 2026), and Medline Convenience Kits Recall (August 11, 2026).

How to tell if you have this one

Check for the UPC 45713-58000 and lot number 1917802 on the packaging. The product is a sterile 4" x 4" wound dressing sold by Southwest Technologies.

  • Brand
    Southwest Technologies
  • Product
    Elasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Sterile. UPC 45713-58000 Bacteriostatic
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check for Mold Contamination

    Inspect the dressing for visible mold growth or unusual odors. If mold is present, discard the dressing immediately.

Where it went and when

Where it was distributed

Distributed in 9 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: yesKSArkansas: not listedARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “CA, GA, IL, KS, NY, OH, TN, TX, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Georgia, Illinois, Kansas, New York, Ohio, Tennessee, Texas, Virginia.

Recall timeline

FDA terminated this recall 4.8 years after the firm started it.

1. Firm started the recall: Nov 18, 201912. FDA classified it Class II: Dec 13, 201923. Published in FDA’s Enforcement Report: Dec 25, 201934. FDA terminated the recall: Aug 23, 2024420192024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The product may be contaminated with mold, so it is not safe to use without checking for mold first.

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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-0687-2020 (November 18, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0687-2020 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA