FDA Medical Device Recalls (openFDA)
Beckman Coulter Inc: Power Processor Aliquot Tube Labels Part 800255
- Recall number
- Z-1154-04
- Recalling firm
- Beckman Coulter Inc
- Product
- Power Processor Aliquot Tube Labels Part 800255
- Status
- Terminated
- Initiated
- 2003-06-23
- Posted
- 2004-07-23
- Terminated
- 2004-08-30
- Reason
- Labels are missing an expiration date and storage instructions, increasing the likelihood that they will not be used by the expiration date or may be stored under conditions that would cause adhesive failure and loss of identity of sample or aliquot during testing.
- Root cause
- Other
- Action
- not on file
- Quantity
- 170 rolls
- Distribution
- not on file
- Lot, serial or model codes
- Lots 21045673; 2105246; 21361906.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- not on file
- Firm FEI
- 2050012
- Firm city
- Brea
- 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