RecallRadar

FDA Device recall Z-2206-2017

Herpes Simplex Virus II 0.5 ml catalog number 362A-15 7.0 mL Catalog number362A-18 . Microbiology - Analyte Specific Reagent In vitro diagn…

On 2017-06-07 the FDA classified a Class II recall of Herpes Simplex Virus II 0.5 ml catalog number 362A-15 7.0 mL Catalog number362A-18 . Microbiology - Analyte Specific Reagent In vitro diagn… by Cell Marque, citing cell Marque has determined the need to issue a product recall after identifying product intended to be sold outside the U.S. was not properly labeled as "For Export Only" as requi….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2206-2017
ClassificationClass II
Statusterminated
Initiated2017-05-05
Published2017-06-07
Last updated2026-09-13 11:54 UTC
CompanyCell Marque
DistributionUS

Product

Herpes Simplex Virus II 0.5 ml catalog number 362A-15 7.0 mL Catalog number362A-18 . Microbiology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent

Reason

Cell Marque has determined the need to issue a product recall after identifying product intended to be sold outside the U.S. was not properly labeled as "For Export Only" as required by section 801 (e )(1) of the FD&C Act.

Identifiers

code_info0.5 ml lot 1512811A, Expiry 201 8-04; 7.0 ml lot 1512810E, expiry 2018-04.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2206-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.