FDA Medical Device Recalls (openFDA)
Stryker Communications Corp: MMP 200 Articulating Booms, Catalog Number 0682-000-604SX, Product Number 0682-001-060C. Used for operating room equipment.
- Recall number
- Z-1611-2011
- Recalling firm
- Stryker Communications Corp
- Product
- MMP 200 Articulating Booms, Catalog Number 0682-000-604SX, Product Number 0682-001-060C. Used for operating room equipment.
- Status
- Terminated
- Initiated
- 2011-01-28
- Posted
- 2011-03-08
- Terminated
- 2011-03-30
- Reason
- Utilization of incorrect screws resulted in inadequate thread engagement reducing the load bearing capability of the product.
- Root cause
- Process control
- Action
- Stryker notified consignees verbally on January 28, 2011 and by letter dated February 11, 2011.
- Quantity
- 2
- Distribution
- MA, CO
- Lot, serial or model codes
- Serial numbers 02074510100008 and 0207451010000
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- not on file
- Firm FEI
- 3002975342
- Firm city
- Flower Mound
- 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