XVIVO Organ Chamber REF 19020
Recall
- Recall Number
- Z-1212-2022
- Event Number
- 90143
- Firm
- XVIVO PERFUSION AB Massans Gata 10 Goteborg Sweden
- FEI Number
- 3007710603
- Product Code
- PHO
- Status
- Terminated
- Root Cause
- Under Investigation by firm
- Initiated
- April 8, 2022
- Terminated
- January 30, 2025
Description
XVIVO Organ Chamber REF 19020
The weld seal of the primary pouch was incomplete, and the sterility of the product cannot be ensured/guaranteed.
On or about 04/11/2022, XVIVO Inc. issued an "URGENT- Field Safety Notice" for its XVIVO Organ Chamber via email to customers informing them XVIVO has identified that the primary package for a number of batches may have notable defects in the weld of the bag. The notable defects are unsealed sections of the weld (i.e. the bag is not completely closed). Unsealed sections in the weld may compromise the sterility of the product and therefore it is important to NOT use a product showing this defect. Customer are instructed to: 1. Carefully check the primary package for unsealed sections. A follow-up "URGENT:-Medical Device Correction" issued on or about 05/06/2022, this letter provides photos of example of unsealed welds. 2. If unsealed sections are noted, do not use the product and contact XVIVO Customer Support at [email protected] for further action. 3. if not defects are noted, the product may be used as intended. Any questions or additional information, contact Customer Support at [email protected] or telephone number +1-303-395-9171.
U.S.: CA, FL, MA, NC, NY, OH, PA, and TX O.U.S.: Austria, Canada, France, Ireland, Italy, and the Netherland
80 devices