FDA Medical Device Recalls (openFDA)
X-Cel X-Ray Corp: X-Cel MB-700 A/C Podiatry X-Ray System; X-Cel X-Ray Coporation, 4220 Waller Drive, Crystal Lake, IL 60012
- Recall number
- Z-0424-03
- Recalling firm
- X-Cel X-Ray Corp
- Product
- X-Cel MB-700 A/C Podiatry X-Ray System; X-Cel X-Ray Coporation, 4220 Waller Drive, Crystal Lake, IL 60012
- Status
- Terminated
- Initiated
- 2002-11-12
- Posted
- 2003-03-05
- Terminated
- 2003-02-28
- Reason
- The X-Ray system contained a defective X-Ray tube shield.
- Root cause
- Other
- Action
- Recalled by telephone call on 11/19/2002, with follow-up visits and letters dated 2/27/03. The tube shields were replaced and the x-ray units were recertified.
- Quantity
- 3 units
- Distribution
- Northbrook, IL and Frankfort, IL
- Lot, serial or model codes
- Model MB-700 A/C, srial numbers 622686, 622687, 622688, 622689, 320367, 325120
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- KPR--
- Firm FEI
- 1418484
- Firm city
- Crystal Lake
- Firm state
- IL
- 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
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
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