FDA Medical Device Recalls (openFDA)
Ortho8, Inc.: EVEXIA LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF(s): EVE-11/EVE-X11, Rx Only, Not Sterile
- Recall number
- Z-2325-2021
- Recalling firm
- Ortho8, Inc.
- Product
- EVEXIA LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF(s): EVE-11/EVE-X11, Rx Only, Not Sterile
- Status
- Open, Classified
- Initiated
- 2021-07-09
- Posted
- not on file
- Terminated
- not on file
- Reason
- EVEXIA LUXE DVT PREVENTION DEVICE is marketed without FDA clearance
- Root cause
- Unknown/Undetermined by firm
- Action
- On July 19, 2021 Ortho8 Inc. issued a "Urgent Medical Device Recall" notification to all affected consignees and users via UPS. In addition to informing consignees/users about the recalled device the firm asked consignees to take the following actions: Consignees: 1. Ortho8 is requiring the immediate return all remaining inventory of Evexia" & Circul8 Luxe devices. All consignees are asked to quarantine and discontinue use of the Evexia" and Circul8 Luxe devices. 2. This recall notice needs to be passed on to all those who need to be aware within your organization or to any organization where the affected devices have been transferred. If your firm distributed the devices to other distributors, you are asked to provide your customers with a copy of this recall notification. If your firm distributed the devices to patients, you are asked to provide these patients with a copy of this recall notification and let them know Ortho8 will replace their device with a Circul8 Pro, a DVT prevention device that has been cleared for marketing by the U.S. FDA. 3. Please complete & return the enclosed acknowledgment form no later than July 30, 2021 and indicate the number of devices being returned Patients: 1. Our records show you received one of these devices. 2. Ortho8 will replace your device with a Circul8 Pro, a DVT prevention device that has been cleared for marketing by the U.S. FDA. 3. We ask that you complete the enclosed acknowledgement form and return to us no later than July 30, 2021. This acknowledgment form will let us know to send you a replacement device. When we send your replacement device, we will also send you a prepaid, addressed package for returning your Evexia" or Circul8 Luxe. 4. Replacement devices will be available to you through September 30, 2021. 5. Meanwhile, consult your physician on identifying other comparable devices to use until your replacement device arrives.
- Quantity
- not on file
- Distribution
- US Nationwide distribution in the states of Al, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MO, NC, NV, NJ, NY, OK, PA, SC, TN, TX, UT, VA.
- Lot, serial or model codes
- All Lots
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JOW
- Firm FEI
- 3016000973
- Firm city
- Rocklin
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28