FDA Medical Device Recalls (openFDA)
Multidata Systems Intl Corp: Block Mold Cutter, Model 8532, Version 1.2.
- Recall number
- Z-0985-02
- Recalling firm
- Multidata Systems Intl Corp
- Product
- Block Mold Cutter, Model 8532, Version 1.2.
- Status
- Terminated
- Initiated
- 2002-11-10
- Posted
- 2003-09-13
- Terminated
- 2003-12-12
- Reason
- The units lacked the required labels per the laser performace standard.
- Root cause
- Other
- Action
- not on file
- Quantity
- 10 units
- Distribution
- Distribution was made to SC, FL, GA, NY, PA, NC, IL, and NJ.
- Lot, serial or model codes
- Serial numbers 20128306, 23073201, 21118501, 20023201, 21118502, 21033201, 20028306, 23093201, 22083201, and 20093201
- 510(k) numbers
- ["K964167"]
- PMA numbers
- not on file
- Product code
- not on file
- Firm FEI
- 1938060
- Firm city
- St Louis
- Firm state
- MO
- 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