| Class 2 Device Recall Access Free T4 Calibrator | |
Date Initiated by Firm | November 11, 2010 |
Date Posted | April 11, 2011 |
Recall Status1 |
Terminated 3 on July 11, 2012 |
Recall Number | Z-1945-2011 |
Recall Event ID |
58163 |
510(K)Number | K982250 |
Product Classification |
Radioimmunoassay, free thyroxine - Product Code CEC
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Product | Access Free T4 Calibrator, Part Number: 33885, Lot Numbers: 014769
The Access Free T4 Calibrators are intended to calibrate the Access Free T4 assay for the quantitative determination of free thyroxine levels in human serum and plasma (heparin) using the Access Immunoassay Systems |
Code Information |
Lot Numbers: 014769 |
Recalling Firm/ Manufacturer |
Beckman Coulter Inc. 200 S Kraemer Blvd Brea CA 92821-6208
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For Additional Information Contact | Clair K. ODonovan, Ph.D. 714-961-4483 |
Manufacturer Reason for Recall | The recall was initiated because the stability claim for Access Free T4 calibrator lot 014769 is not met. The affected T4 calibrator lot can produce quality control and patient results that are erroneously low (by greater than 2 standard deviations). An erroneously low patient result may lead to misdiagnosis and/or delayed treatment. |
FDA Determined Cause 2 | Other |
Action | The firm, Beckman Coulter, sent an "URGENT: PRODUCT CORRECTIVE ACTION" (PCA) letter dated November 29, 2010 to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to do the following:
ACTION/RESOLUTION:
" Discontinue use of Access Free T4 calibrator lot 014769.
" Review historical quality control performance and determine whether any reported patient results were obtained while using a faulty calibration. If results were affected, you will see a shift downward in control recovery that produces out-of-range low QC results.
" If patient results were obtained with Access Free T4 calibrator lot number 014769, it is possible they are erroneously low. If any patient results were reported in the period between the time the erroneous calibration with the affected lot was performed and when a different calibrator lot was used, the laboratory should consider advising physicians to whom results were reported so they can evaluate whether diagnosis or treatment decisions should be revisited.
" No further orders of Access Free T4 Calibrator lot number 014769 will be shipped. Alternate lots will be provided for current and future replenishment orders or requests.
Consignees/customers were asked to share this information with laboratory staff and retain this notification as part of their laboratory Quality System documentation; and complete and return the enclosed RESPONSE FORM via fax to Beckman Coulter at 786-639-4000.
For product replacement:
" In the United States, please contact Client Services at 1-800-526-3821, option 1.
" In Canada, please contact Customer Service at 1-800-463-7828.
" Outside of the United States and Canada, contact local Beckman Coulter representative.
Questions and answers regarding this issue were enclosed for consignee/customer reference. Additional questions, were directed to the Customer Support Center on the Beckman Coulter website at http://www.beckmancoulter.com/customer |
Quantity in Commerce | 459 units |
Distribution | Worldwide distribution: USA and countries including: Argentina, Belgium, Bosnia and Herzegovina, Canada, China, Colombia, Czech Republic, French Polynesia, Hong Kong, Ireland, Israel, Japan, Jordan, Kuwait, Malaysia, Mexico, Oman, Panama, Philippines, Russian Federation, South Africa, Switzerland, Taiwan, Thailand, Tunisia, United Kingdom, Venezuela, and Zambia. |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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510(K) Database | 510(K)s with Product Code = CEC
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