Dual Lumen Cannula, 12Fr., sterile, disposable. Manufactured by OriGen Biomedical, 4020 S. Industrial Dr. #160, Austin,
FDA device recall Z-0055-06 · posted 2005-10-15 · Terminated
Recall details
- Recalling firm
- Origen Biomedical, Inc
- Reason for recall
- Leak between two lumens causes reduced performance.
- Action taken
- The recall was initiated by letter to all consignees on 12/16/2002.
- Root cause
- Other
- Status
- Terminated
- Product code
- DQO
- Quantity affected
- 170 catheters
- Distribution
- The product was distributed to healthcare facilities and institutions in NC, OH, TX, CA, MO, MI, MN, LA, PA, WA, GA, RI, MD, TN, MA, KY, OR, FL, and WI. The product was distributed to the following fo
- Date initiated
- 2002-12-16
- Date posted
- 2005-10-15
- Date terminated
- 2005-11-03
- Location
- Austin, TX
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