FDA Medical Device Recalls (openFDA)
Global Focus Marketing & Develop: Global Focus Marketing and Distribution, Silencer S2200 Centrifuge
- Recall number
- Z-2857-2011
- Recalling firm
- Global Focus Marketing & Develop
- Product
- Global Focus Marketing and Distribution, Silencer S2200 Centrifuge
- Status
- Terminated
- Initiated
- 2011-07-15
- Posted
- 2011-07-27
- Terminated
- 2013-11-06
- Reason
- Potential for bucket and insert not seated on the rotor to cause the lid to break and buckets to be ejected.
- Root cause
- Nonconforming Material/Component
- Action
- Global Focus Marketing and Distribution, Ltd issued a press release on 07/19/11 and a URGENT: DEVICE RECALL letter was mailed to the firm's customers on 07/15/11 and 07/21/11. Discontinue use. For questions, contact: (800) 323-4306 or silencer@gfmd.com
- Quantity
- 859 units
- Distribution
- Worldwide to USA, United Kingdom, Ireland, Canada, and China.
- Lot, serial or model codes
- Serial numbers: 0493128 through 0798286, 98267203 through 06067205, and 04084R01 through 09274R01.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JQC
- Firm FEI
- 1000599190
- Firm city
- Dallas
- Firm state
- TX
- 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