Single Analyte Urine DAU Control (5 m L Norbuprenorphine, Level II control For In Vitro Diagnostic Use Only. store at 2
FDA device recall Z-0386-2014 · posted 2013-11-25 · Terminated
Recall details
- Recalling firm
- Lin-Zhi International Inc
- Reason for recall
- Product catalog # A68825 Norbuprenorphine 13 ng/mL Level 2 Controls gives a decreased concentration reading due to the degradation of the NBUP analyte in solution.
- Action taken
- Beckman Coulter sent a Manufacturer Field Action Letter dated November 2013, to the one distributor. The letter identified the product the problem and the action needed to be taken by the customer. Please share this information with your laboratory staff and retain this notification as part of your laboratory Quality System documentation. If you have forwarded any of the affected product(s) listed above to another laboratory, please provide them a copy of this letter. If you have any questions regarding this notice, please contact our Customer Support Center Via our website, http://www.beckmancoulter.com/customersupport/support Via phone, call 1-800-854-3633 in the United States Outside the United States, contact your local Beckman Coulter Representative. We apologize for any inconvenience.
- Root cause
- Under Investigation by firm
- Status
- Terminated
- Product code
- LAS
- Quantity affected
- 60 items
- Distribution
- US Distribution in CA.
- Date initiated
- 2013-10-03
- Date posted
- 2013-11-25
- Date terminated
- 2013-12-26
- Location
- Sunnyvale, CA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| BUPRENORPHINE ENZYME IMMUNOASSAY, CALIBRATORS AND CONTROLS FOR BECKMAN COULTER SYNCHRON SYSTEMS (K081008) | Lin-Zhi International, Inc. | 2008-12-22 |