Access Ostase QC, Part Number: 37309. The Access Ostase QC is intended for monitoring system performance of the Access O
FDA device recall Z-1239-2012 · posted 2012-03-21 · Terminated
Recall details
- Recalling firm
- Beckman Coulter Inc.
- Reason for recall
- The recall was initiated because Beckman confirmed that the Access Ostase Calibrator and QC lots do not meet expiration date claims. The Access Ostase Reagent Kit lots identified were quality control tested and released using Access Ostase Calibrator and QC lots that contain the implicated raw material.
- Action taken
- Beckman Coulter sent an "URGENT PRODUCT CORRECTION" letter dated November 9, 2011 to all affected customers. The letter identifies the product, problem, and actions to be taken by the customers. The letter instructs customers to discontinue use and discard all remaining inventory. In addition, a Response Form was enclosed for customers to complete and return. Contact Beckman's Customer Support Center at (800) 854-3633 for questions regarding this notice.
- Root cause
- Process design
- Status
- Terminated
- Product code
- JJX
- Quantity affected
- 4961 units total (1321 units in US)
- Distribution
- Worldwide Distribution-USA (nationwide) and the countries of Algeria, Argentina, Australia, Austria, Belgium, Canada, China, Colombia, Czech Republic, Denmark, France, Georgia, Germany, Greece, Hong K
- Date initiated
- 2011-11-10
- Date posted
- 2012-03-21
- Date terminated
- 2012-06-26
- Location
- Brea, CA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| ACCESS OSTASE QC (K994277) | Beckman Coulter, Inc. | 2000-01-14 |