Recall Z-0883-06 ยท DAP Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control
Dade Behring , Inc.
Stratus CS STAT Fluorometric Analyzer DDMR DilPak (CDDMR-D) in vitro diagnostic.
| Date | May 19, 2006 (initiated Apr 3, 2006) |
| Status | Terminated |
| Reason | Foil sealing of the DilPak may occlude the pipet tip resulting in insufficient aspiration of fluids. Erroneous test results may be generated without an associated error code. Test results may be falsely elevated or depressed, and the magnitude of the inaccuracy may vary based on the degree of occlusion. |
| Root cause | Other |
| Action | Customers were provided clear written instructions (04/06/2006) to discontinue use and discard remaining inventory of products over 2 months old. In addition, each customer is being contacted by phone as an effectiveness verification. Recalling firm is also instructing Stratus CS customers to process all samples and dilutions in duplicate. |
| Quantity | 419 cartons of 5 DilPaks |
| Distribution | Nationwide to hospitals and government accounts in addition to International accounts in Canada, Saudi Arabia, Bangladesh, UAE, India, Japan, Denmark, and Australia. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K022976 | STRATUS CS D-DIMER (DDMR) METHOD (TESTPAK & DILPAK), MODELS CDDMR & CDDMR-D Dade Behring, Inc., Jan 16, 2003 |