FDA recall record

EHOB Econocare Plus Overlay Item: 1025EC recall — FDA Z-1457-2020

Due to a nonconformance of product contamination (human blood) of Econocare Plus Waffle Overlay products with the (master) lot # 932213A that may affect a…

Class IIclassification
Z-1457-2020official record ID
Mar 18, 2020report date

Recall record at a glance

Official recordZ-1457-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEHOB, Inc.
Report dateMar 18, 2020
Recall initiation dateJan 19, 2020
QuantityU.S. (TX)
LocationIndianapolis, IN, United States

Official product description

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.

Why the product was recalled

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.

Distribution information

US Nationwide distribution in the state of TX.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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