Z-1639-2011

HSV-1 IgG ELISA kit ; HSV-1 IgM ELISA kit; BioCheck, Foster City, CA 9440. Quantitative determination of AFP...

Name: Z-1639-2011 HSV-1 IgG ELISA kit ; HSV-1 IgM ELISA kit; BioCheck, Foster City, CA 9440. Quantitative determination of AFP...
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 HSV-1 IgG ELISA kit ; HSV-1 IgM 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-1639-2011
Status: Terminated
Initiated: 2010-12-22
Posted: 2011-03-11
Terminated: 2011-03-25
Recalling firm: BioCheck Inc
Product: HSV-1 IgG ELISA kit ; HSV-1 IgM ELISA kit; BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum.
Product code: LGC Enzyme Linked Immunoabsorbent Assay, Herpes Simplex Virus, Non-Specific
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).
Quantity in commerce: estimate 25,000 total kits, all varieties.
Distribution: Nationwide distribution.
Product codes and lots: Catalog number: BC-1093: RN-33786 03-2010 RN-33956 03-2010 RN-34538 03-2010 RN-35037 08-2010 RN-35242 09-2010 RN-36114 12-2010 RN-37937 03-2011 RN-38809 07-2011 RN-38839 06-2011 RN-39279 09-2011 RN-40515 02-2012 RN-40515A 02-2012 N-40833 02-2012 RN-40835 02-2012 RN-41271 02-2012 RN-41301 02-2012 RN-41357 02-2012; Catalog number BC-1095: RN-33990 04-2010 RN-34548 02-2010 RN-34904 04-2010 RN-35427 09-2010 RN-35807 10-2010 RN-35889 10-2010 RN-37713 03-2011 RN-38218 04-2011 RN-38875 07-2011 RN-39471 10-2011 RN-40226 10-2011 RN-40226A 10-2011 RN-40516 03-2012 RN-40942 03-2012 RN-41214 03-2012.

Product code LGC

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)