FDA Medical Device Recalls (openFDA)
Stryker Instruments Div. of Stryker Corporation: Stryker PainPump1 1-Day Infusion Kit; Product number 500-140-000.
- Recall number
- Z-0665-06
- Recalling firm
- Stryker Instruments Div. of Stryker Corporation
- Product
- Stryker PainPump1 1-Day Infusion Kit; Product number 500-140-000.
- Status
- Terminated
- Initiated
- 2006-02-03
- Posted
- 2006-03-21
- Terminated
- 2007-06-04
- Reason
- The catheter tubing included in the kit may break during removal.
- Root cause
- Other
- Action
- Each consignee was notified of the recall via recall letter dated 2/7/06, which requested that they destroy the affected lots on site. International accounts were notified via email.
- Quantity
- not on file
- Distribution
- Nationwide, Australia and Canada.
- Lot, serial or model codes
- Lot 2005051101 and 2005062301.
- 510(k) numbers
- ["K042405"]
- PMA numbers
- not on file
- Product code
- MEA
- Firm FEI
- 1811755
- Firm city
- Portage
- Firm state
- MI
- 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