RegWardenFDA facility compliance records
Recall

Class II — EHOB, Inc.

Recalling firmEHOB, INC.
Registered facilityView this company's 5 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusOngoing
ReasonProduct contamination-a trace amount of dried bodily fluids may expose patients, health care providers to contaminates
ProductEconocare Plus Waffle Overlay- Intended for use as a medical device to aid in the prevention and treatment of pressure injuries or bed sores and general comfort. Product Code: 1025ECP
Quantity70 units
DistributionUS Nationwide distribution in the states of AZ, IN, ME, NE, OH, SD.
Initiated2021-04-19
Classified2021-06-24
Recall numberZ-1950-2021
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — EHOB, Inc. (Z-1950-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/87864/

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