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FDA Medical Device Recalls (openFDA)

Beckman Coulter Inc.: 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

Recall number
Z-1945-2011
Recalling firm
Beckman Coulter Inc.
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
Status
Terminated
Initiated
2010-11-11
Posted
2011-04-11
Terminated
2012-07-11
Reason
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.
Root cause
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
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.
Lot, serial or model codes
Lot Numbers: 014769
510(k) numbers
["K982250"]
PMA numbers
not on file
Product code
CEC
Firm FEI
2050012
Firm city
Brea
Firm state
CA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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