RecallRadar

FDA Device recall Z-0439-2016

Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for determining the antimicrob…

On 2015-12-30 the FDA classified a Class I recall of Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for determining the antimicrob… by Biomerieux, citing due to the potential for reporting erroneous results for Piperacillin/Tazobactam; specifically false susceptible results.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0439-2016
ClassificationClass I
Statusterminated
Initiated2015-11-19
Published2015-12-30
Last updated2026-09-13 11:53 UTC
CompanyBiomerieux
DistributionUS

Product

Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria.

Reason

Due to the potential for reporting erroneous results for Piperacillin/Tazobactam; specifically false susceptible results.

Identifiers

code_infoRef. 412434, Lot numbers: 1004331500, 1004271120, 1004178060, 1003977300, 1003697470, 1003415090, 1003276060, 1003069230, 1002488490 and 1001936360.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0439-2016%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.