FDA Recall
Completed
Spiral Gold Hollow Fiber Oxygenator with Duraflow Treatment, a hollow fiber membrane oxygenator.
Recall: Z-0312-03
·
Initiated November 1, 2002
Recall
- Recall Number
- Z-0312-03
- Event Number
- 25002
- Firm
- Jostra-Bentley Corporation
- Status
- Completed
- Initiated
- November 1, 2002
- Address
- 2828 North Cresent Ridge Dr, The, Woodlands, 77381-3902
Description
Spiral Gold Hollow Fiber Oxygenator with Duraflow Treatment, a hollow fiber membrane oxygenator.
Reason
Separation between lid and housing unit.
Action
Accounts notified by phone 10/9/02 and letter 11/1/02. Recalling firm is requesting return of the recalled product.
Distribution
OH, KY, AL, TN, FL, NY, IL, no government or military accounts
Quantity
356 units