Data Foundry

Medical device recalls 2017

TrypticaseTM Soy Agar with 5% Sheep Blood — Class II medical device recall Z-0196-2018

Terminated recall by Becton Dickinson & Co., reported 2017-12-13, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Listeria monocytogenes contamination of non-sterile plated media

Recall numberZ-0196-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBecton Dickinson & Co., Sparks, MD, United States
Recall initiated2017-05-22
Classified2017-12-06
Reported by FDA2017-12-13
Terminated2018-02-26
DistributedAK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GU, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA
Countries outside the USCA, JP
Reason classesmicrobial contamination, sterility
Pathogenslisteria monocytogenes
Lot numbers7032978, 7048902
Model numbers221261
Expiration dates2017-05-24, 2017-06-09

Product

TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM), Catalog Number 221261 Trypticase Soy Agar with 5% or 10% Sheep Blood is used for cultivating fastidious microorganisms and for the visualization of hemolytic reactions produced by many bacterial species.

Reason for recall

Listeria monocytogenes contamination of non-sterile plated media

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0196-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.