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Lower risk Medical device recall · FDA · Published April 19, 2021

EHOB Econocare Plus Waffle Overlay Recall: Risk of Contamination from Dried Bodily Fluids

EHOB recalls Econocare Plus Waffle Overlay medical devices due to potential contamination from dried bodily fluids. This may expose patients and healthcare providers to contaminants. Affected units have product code 1025ECP and lot number 10501:13A.

🇺🇸 FDA recall #Z-1950-2021Medical deviceEHOB ›
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Recalling firmEHOB, Inc.250 N Belmont Ave · Indianapolis, IN 46222-4265
✎ GovInfoNow plain-language explainer

EHOB is recalling Econocare Plus Waffle Overlay medical devices because a trace amount of dried bodily fluids could contaminate the product. This poses a risk of exposure to patients and healthcare providers. The recall affects specific product codes and lot numbers. Read more at govinfonow.com/recall/62767-ehob-econocare-plus-waffle-overlay-recall-risk-of-contamination-from.

Source Summary by GovInfoNow · govinfonow.com/recall/62767-ehob-econocare-plus-waffle-overlay-recall-risk-of-contamination-from · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1950-2021

Cite this page

“EHOB Econocare Plus Waffle Overlay Recall: Risk of Contamination from Dried Bodily Fluids.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62767-ehob-econocare-plus-waffle-overlay-recall-risk-of-contamination-from. Based on FDA recall #Z-1950-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1950-2021%22&limit=1).

The FDA announced on April 19, 2021, that EHOB, Inc. is recalling Econocare Plus Waffle Overlay medical devices due to potential contamination by dried bodily fluids. The agency issued recall number Z-1950-2021 for the Class II device distributed nationwide.

How to tell if you have it

  • Brand: EHOB
  • Product: Econocare Plus Waffle Overlay
  • Product Code: 1025ECP
  • Lot Number: 105013A
  • Quantity: 70 units

The hazard

The recall addresses product contamination where a trace amount of dried bodily fluids may expose patients and health care providers to contaminants. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show EHOB, Inc. has two other recalls on record since January 19, 2020. On June 9, 2020, EHOB recalled a Waffle Overlay due to a blood contamination risk observed during QC inspection. On January 19, 2020, the company recalled Econocare Plus Overlay products due to nonconformance involving human blood contamination in lot #932213A. Other recent recalls of similar products include Medline Convenience Kits Recall: Contaminated Components Risk (July 10, 2026) and Medline Convenience Kits Recall: Risk of Microbial Contamination from Packaging Wrinkles (June 12, 2026).

How to tell if you have this one

Check for product code 1025ECP and lot number 105013A on the Econocare Plus Waffle Overlay device. This medical device is intended for pressure injury prevention and bed sore treatment.

  • Brand
    EHOB
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for product code 1025ECP and lot number 105013A on the device.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 6 states.

Alaska: nationwideAKMaine: named in the noticeMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: nationwideWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: nationwideILWisconsin: nationwideWIMichigan: nationwideMINew York: nationwideNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: nationwideORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: named in the noticeSDIowa: nationwideIAIndiana: named in the noticeINOhio: named in the noticeOHPennsylvania: nationwidePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: nationwideCAUtah: nationwideUTColorado: nationwideCONebraska: named in the noticeNEMissouri: nationwideMOKentucky: nationwideKYWest Virginia: nationwideWVVirginia: nationwideVAMaryland: nationwideMDDelaware: nationwideDEArizona: named in the noticeAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: nationwideARTennessee: nationwideTNNorth Carolina: nationwideNCSouth Carolina: nationwideSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: nationwideGAHawaii: nationwideHITexas: nationwideTXFlorida: nationwideFL

FDA distribution: “US Nationwide distribution in the states of AZ, IN, ME, NE, OH, SD.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Arizona, Indiana, Maine, Nebraska, Ohio, South Dakota.

Recall timeline

FDA published this recall 2 months after the firm started it.

1. Firm started the recall: Apr 19, 202112. FDA classified it Class II: Jun 24, 202123. Published in FDA’s Enforcement Report: Jun 30, 202132021
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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 #Z-1950-2021 (April 19, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1950-2021 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