Equal Diagnostics Lipase Color Reagent Kit Part Number: 905-D For In Vitro Diagnostic Use Containing the Lipase Color Re
FDA device recall Z-2150-2008 · posted 2008-08-22 · Terminated
Recall details
- Recalling firm
- Genzyme Corporation
- Reason for recall
- Calibration and Quality Control outside of established range resulting from an increase in initial OD readings with the reagent contained within the kits.
- Action taken
- Genzyme notified accounts by Fed'X on 4/14/08 via an Imprtant Field Correction letter, requesting users to discard kits and follow the "User Update" instructions previously provided to minimize calibration error. Customers are to complere and sign the Confirmation of Notification form and fax it back to the firm regardless if they have any affected product or not. Also, requires that the customer confirms that the REagent OD limits for First and Last H are set at 0.15 for Lipase on the Olympus AU400/400e, AU600, AU640/640e and AU2700/AU5400 Systems.
- Root cause
- Nonconforming Material/Component
- Status
- Terminated
- Product code
- CHI
- Quantity affected
- 3,443
- Distribution
- Nationwide Distribution
- Date initiated
- 2008-04-14
- Date posted
- 2008-08-22
- Date terminated
- 2008-09-16
- Location
- Cambridge, MA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| LIPASE COLOR [TOYO] SERUM LIPASE TEST KIT (K897150) | Toyo Jozo Co., Ltd. | 1990-02-26 |