Z-1629-2011

CA15-3 ELISA Kit. BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human...

Name: Z-1629-2011 CA15-3 ELISA Kit. BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human...
Creator: BioCheck Inc
Published: 2010-12-22
License: https://open.fda.gov/license/

BioCheck Inc / initiated 2010-12-22 / Terminated / root cause: labeling and UDI

FDA source

BioCheck Inc began a recall of CA15-3 ELISA Kit. BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum on 2010-12-22. The reason FDA records is "Product labels indicate that the products are for IVD use and they do not have an approved 510(k)". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-1629-2011
Status: Terminated
Initiated: 2010-12-22
Posted: 2011-03-11
Terminated: 2011-03-25
Recalling firm: BioCheck Inc
Product: CA15-3 ELISA Kit. BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum.
Product code: LTK Test, Epithelial Ovarian Tumor-Associated Antigen (Ca125)
Reason for recall: Product labels indicate that the products are for IVD use and they do not have an approved 510(k).
Root cause tag: labeling and UDI
FDA root cause: PMA
Action: The firm, BioCheck, sent an "URGENT: DEVICE RECALL" letter dated December 22, 2010 to all customers. The letter described the product, problem and actions to be taken by customers. The customer were instructed to examine their inventory for the affected lots, if found, discontinue distributing the lots and promptly return via Fedex to BioCheck at 323 Vintage Park Drive, Foster City, CA 94404, Attn: RETURNED GOODS; immediately contact their accounts, if they further distributed the product, and inform them of the Recall, and complete and return the response form via email at: [email protected] or fax to (650-573-1969) immediately. If you have any questions, please call (650) -573-1968 anytime during office hours (8:30am to 5:30pm Pacific time).
Distribution: Nationwide distribution.
Product codes and lots: Catalog number: BC-1015; RN-33788 03-2010 RN-34315 06-2010 RN-34585 06-2010 RN-34802 07-2010 RN-34848 06-2010 RN-34849 07-2010 RN-35139 08-2010 RN-35352 07-2010 RN-35761 09-2010 RN-36390 12-2010 RN-36607 12-2010 RN-36869 02-2011 RN-37038 02-2011 RN-37446 04-2011 RN-37902 02-2011 RN-38216 07-2011 RN-38808 07-2011 RN-39616 10-2011 RN-40296 02-2012 RN-40393 02-2012 RN-41007 04-2012

Product code LTK

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)