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FDA Medical Device Recalls (openFDA)

Siemens Healthcare Diagnostics, Inc: ADVIA Centaur iPTH Calibrator 2 pk; REF 10492394. For in vitro diagnostic use in calibrating Intact PTH assays.

Recall number
Z-1514-2013
Recalling firm
Siemens Healthcare Diagnostics, Inc
Product
ADVIA Centaur iPTH Calibrator 2 pk; REF 10492394. For in vitro diagnostic use in calibrating Intact PTH assays.
Status
Terminated
Initiated
2013-05-14
Posted
2013-06-06
Terminated
2015-03-05
Reason
iPTH Assay- reagent and calibrator lots may have demonstrated higher than anticipated variability
Root cause
No Marketing Application
Action
Siemens sent an Urgent Medical Device Correction letter dated May 2013 to all affected customers. The letter identified the product, problem, and actions to be taken by the customers. For questions, contact your Siemens Technical Solutions Center or your local Siemens technical support.
Quantity
99 (2 pk)
Distribution
Nationwide Distribution.
Lot, serial or model codes
Calibrator Lot Number: C5601 and C5602 Kit Lot Number/Exp. Date: 61405A01 27 Oct 2011 66517A02 27 Oct 2011 66611A02 27 Oct 2011 71997C02 27 Oct 2011
510(k) numbers
["K020217"]
PMA numbers
not on file
Product code
JIT
Firm FEI
1219913
Firm city
East Walpole
Firm state
MA
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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