SSCOR Suction Device Model 2314B
FDA device recall Z-0415-05 · posted 2005-01-27 · Terminated
Recall details
- Recalling firm
- S S C O R Inc
- Reason for recall
- 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.
- Action taken
- SSCOR Powered Suction Device not performing as intended.
- Root cause
- Other
- Status
- Terminated
- Product code
- BTA
- Quantity affected
- 196
- Distribution
- CA, FL, IA, IL, IN, KY, MO, NC, NJ, NY, OH, France, New Zealand, Singapore, United Kingdom
- Date initiated
- 2005-01-06
- Date posted
- 2005-01-27
- Date terminated
- 2011-06-13
- Location
- Sun Valley, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.