Severity
Moderate
FDA Devices recall · Reported March 18, 2020
Due to a nonconformance of product contamination (human blood) of Econocare Plus Waffle Overlay products with the (master) lot # 932213A that may affect a subset of the lot- contr…
Ehob, Inc. recalled Econocare Plus Overlay Item: 1025EC. Intended to aid in the prevention and treatment of … - a moderate-severity action.
Econocare Plus Overlay Item: 1025EC. Intended to aid in the prevention and treatment of … was recalled by Ehob, Inc. in March 18, 2020. Reason: Due to a nonconformance of product contamination (human blood) of Econocare Plus Waffle Overlay products with…. Check the official notice for the remedy. Verify recall #Z-1457-2020 with the FDA Devices before acting.
The recall
Ehob, Inc. issued this moderate-severity FDA Devices recall-Due to a nonconformance of product contamination (human blood) of Econocare Plus Waffle Overlay products with….
Sourced from official FDA Devices enforcement records. Verify recall #Z-1457-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Devices action (record #Z-1457-2020) was formally reported on March 18, 2020, with the manufacturer initiating the action on January 19, 2020. It is classified under Moderate severity (Class II), with a current status of Terminated. Ehob, Inc. is listed as the recalling firm, operating out of Indianapolis, IN. Federal records list the affected scope as U.S. (TX).
The documented reason for this recall is: Due to a nonconformance of product contamination (human blood) of Econocare Plus Waffle Overlay products with the (master) lot # 932213A that may affect a subset of the lot- controlled product (# 932243A). This nonconfo… Distribution data in the federal record shows the product reached: US Nationwide distribution in the state of TX.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
U.S. (TX)
Related Recalls
6
3 from same agency
Econocare Plus Overlay Item: 1025EC. Intended to aid in the prevention and treatment of pressure injuries and general comfort - Product Usage: The EHOB WAFFLE Overlay intended use is as first line of defense for pressure injury prevention. The design provides the caregiver a point-of-care solution with the versatility of patient handling and transferring, which encourages ease of use and compliance. The design provides airflow to aid in patient comfort and pressure injury prevention.
Due to a nonconformance of product contamination (human blood) of Econocare Plus Waffle Overlay products with the (master) lot # 932213A that may affect a subset of the lot- controlled product (# 932243A). This nonconformance has the potential to expose the end user to materials deemed to be a health risk. Firm is aware of zero instances of contamination in distributed products that have reached consignees.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1457-2020 |
| Date reported | March 18, 2020 |
| Date initiated | January 19, 2020 |
| Recalling firm | Ehob, Inc. |
| Firm location | Indianapolis, IN |
| Affected scope | U.S. (TX) |
| Distribution | US Nationwide distribution in the state of TX. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported March 18, 2020. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.