RegWardenFDA facility compliance records
Recall

Class II — Life Technologies Corporation

Recalling firmLife Technologies Corporation
Registered facilityView this company's 9 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusTerminated
ReasonFirm received complaints that HSV-2 primers failed to amplify HSV-2 DNA.
ProductHSV 2 Primers, Catalog #18081020. Analyte Specific Reagent. The HSV-2 primer pair is specific for HSV-2 (Herpes Simplex Virus 2). For use in Clinical laboratories when developing their own diagnostic tests.
Quantity15 kits
DistributionUSA Nationwide Distribution in the states of DE, IA, MN, and NC.
Initiated2013-05-13
Classified2013-08-26
Terminated2013-08-28
Recall numberZ-2085-2013
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Life Technologies Corporation (Z-2085-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65770/

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