Data Foundry

Medical device recalls 2018

Difco" Agar Noble — Class II medical device recall Z-0935-2018

Terminated recall by Becton Dickinson & Co., reported 2018-03-21, distributed nationwide. HighPuragar was mislabeled and inadvertently sold as Noble Agar.

Recall numberZ-0935-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBecton Dickinson & Co., Sparks, MD, United States
Recall initiated2017-10-03
Classified2018-03-09
Reported by FDA2018-03-21
Terminated2018-10-09
DistributedNationwide (US)
Quantity216 bottles
Reason classeslabeling
Lot numbers7109502
Model numbers214230

Product

Difco" Agar Noble, 500g bottle Noble Agar is a solidifying agent that is essentially free of impurities. It is used in electrophoretic and nutritional procedures and in preparing microbiological culture media when increased purity is required.

Reason for recall

HighPuragar was mislabeled and inadvertently sold as Noble Agar.

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-0935-2018. 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.