FDA Medical Device Recalls (openFDA)
Stockwell Scientific Inc: 50 mL sterile plastic centerfuge tubes.
- Recall number
- Z-0512-04
- Recalling firm
- Stockwell Scientific Inc
- Product
- 50 mL sterile plastic centerfuge tubes.
- Status
- Terminated
- Initiated
- 2003-12-29
- Posted
- 2004-02-04
- Terminated
- 2004-04-08
- Reason
- Tubes are brittle and break during centerfuging specimens.
- Root cause
- Other
- Action
- Firm sent a recall letter to all customers 12/30/2003 requesting return of existing stock and subrecall of subdistributed product.
- Quantity
- 3762 cases (500 tubes/cs)
- Distribution
- Nationwide and Canada
- Lot, serial or model codes
- Codes 3250, 3250P, 3252, 3252P and the lot numbers: 69766 through 87512 which were manufactured from 02/03/03 - 09/22/2003 Also: 3250-DES1, 3250P-DES1, 3252-DES1, 3252P-DES1 3250P-MIS1, 3252P-MIS1 3250P-USA1, 3252P-USA1
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JKA
- Firm FEI
- 3000013175
- Firm city
- Scottsdale
- Firm state
- AZ
- 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