EHOB, INC.
3 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (3)
- Inspections (1)
Devices registered here (1)
- Aid, TransferProduct code IKX (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.5050
Recalls & enforcement
- Class IIOngoing2021-04-19Product contamination-a trace amount of dried bodily fluids may expose patients, health care providers to contaminates
- Class IITerminated2020-06-09QC inspection observed that a portion of the lot may have been contaminated with blood.
- Class IITerminated2020-01-19Due 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 …
FDA inspections (1)
- VAI2019-05-06Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
- All facilities operated by EHOB, INC.
- EHOB(JiaXing) Medical Product Co., LTD. (CN)
- Shanghai EHOB Health Care Products Co., LTD. (CN)
- EHOB (Shanghai) Medical Products Co. Ltd. (CN)
- EHOB Distribution Center W. 21st Street (IN)
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “EHOB, INC. (FEI 1832066) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1832066-ehob-inc/
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