FDA Medical Device Recalls (openFDA)
S S C O R Inc: SSCOR Suction Device Model 2314B
- Recall number
- Z-0415-05
- Recalling firm
- S S C O R Inc
- Product
- SSCOR Suction Device Model 2314B
- Status
- Terminated
- Initiated
- 2005-01-06
- Posted
- 2005-01-27
- Terminated
- 2011-06-13
- Reason
- Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in questions is caused by cracked regulators that result in inadequate suction.
- Root cause
- Other
- Action
- SSCOR Powered Suction Device not performing as intended.
- Quantity
- 196
- Distribution
- CA, FL, IA, IL, IN, KY, MO, NC, NJ, NY, OH, France, New Zealand, Singapore, United Kingdom
- Lot, serial or model codes
- Serial Number: N00215 - N00407
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- BTA
- Firm FEI
- 2022724
- Firm city
- Sun Valley
- 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