Data Foundry

Medical device recalls 2013

BD BBL CDC Anaerobe 5% Sheep Blood Agar with Kanamycin and Vancomycin — Class II medical device recall Z-1800-2013

Terminated recall by Becton Dickinson & Co., reported 2013-07-31, distributed nationwide. Microbiological identification media may exhibit reduced levels of Vancomycin.

Recall numberZ-1800-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBecton Dickinson & Co., Sparks, MD, United States
Recall initiated2013-06-06
Classified2013-07-24
Reported by FDA2013-07-31
Terminated2013-09-03
DistributedNationwide (US)
Countries outside the USBE, CA, MX, SG, TW
Quantity45 cartons
Reason classesmicrobial contamination
Lot numbers3073075, 3080083
Model numbers221736
Expiration dates2013-05-29, 2013-06-04

Product

BD BBL CDC Anaerobe 5% Sheep Blood Agar with Kanamycin and Vancomycin (KV), packaged in cartons of 100 plates, Catalog # 221736, and labeled in part ***Becton, Dickinson and Company 7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds*** CDC Anaerobe 5% Sheep Blood Agar with Kanamycin and Vancomycin is used for the selective isolation of fastidious and slow-growing, obligately anaerobic gram-negative bacteria from a variety of clinical and nonclinical materials.

Reason for recall

Microbiological identification media may exhibit reduced levels of Vancomycin.

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-1800-2013. 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.