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Lower risk Medical device recall · FDA · Published January 19, 2020

EHOB Econocare Plus Overlay: Risk of Blood Contamination in Some Products

EHOB recalls Econocare Plus Waffle Overlay products (lot 932243A) due to potential blood contamination. This may expose users to health risks. No injuries reported.

🇺🇸 FDA recall #Z-1457-2020Medical deviceEHOB ›
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Recalling firmEHOB, Inc.250 N Belmont Ave · Indianapolis, IN 46222-4265
✎ GovInfoNow plain-language explainer

EHOB is recalling some Econocare Plus Waffle Overlay products because they may contain human blood. This could expose users to health risks, though no injuries have been reported. Read more at govinfonow.com/recall/65975-ehob-econocare-plus-overlay-risk-of-blood-contamination-in-some.

Source Summary by GovInfoNow · govinfonow.com/recall/65975-ehob-econocare-plus-overlay-risk-of-blood-contamination-in-some · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1457-2020

Cite this page

“EHOB Econocare Plus Overlay: Risk of Blood Contamination in Some Products.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65975-ehob-econocare-plus-overlay-risk-of-blood-contamination-in-some. Based on FDA recall #Z-1457-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1457-2020%22&limit=1).

The FDA announced on Jan. 19, 2020, that EHOB, Inc. is recalling Econocare Plus Overlay Item 1025EC due to potential human blood contamination. The agency said the recall addresses a health risk from nonconformance in lot 932213A and product lot code 932243A.

How to tell if you have it

  • Brand: EHOB
  • Product: Econocare Plus Overlay Item 1025EC
  • Master Lot #: 932213A
  • Product Lot Code: 932243A

The hazard

The FDA said the Econocare Plus Waffle Overlay products may have been contaminated with human blood, posing a health risk to end users. The firm is aware of zero instances of contamination in distributed products that have reached consignees.

Context

GovInfoNow's records show EHOB, Inc. has two other recalls on record since June 9, 2020. On April 19, 2021, the company recalled Econocare Plus Waffle Overlay products due to a risk of contamination from dried bodily fluids. Other recent recalls of similar products include Medline Blood Culture Kits Recall (March 16, 2026), Medline Convenience Kits Recall (June 12, 2026), and Medline Blood Culture Kit Recall (Dec. 24, 2025).

How to tell if you have this one

Check for the lot code 932243A on the product. The product is sold under the brand EHOB for pressure injury prevention.

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

What to do — step by step

  1. Check Product Lot Code

    Look for the lot code 932243A on the Econocare Plus Waffle Overlay product.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “US Nationwide distribution in the state of TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Jan 19, 202012. FDA classified it Class II: Mar 9, 202023. Published in FDA’s Enforcement Report: Mar 18, 202034. FDA terminated the recall: Aug 5, 202042020
  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.

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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-1457-2020 (January 19, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1457-2020 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