FDA Device recall Z-1334-2013
BBL(tm) CDC Anaerobe 5% Sheep Blood Agar
- FDA Device
- Class II
- terminated
- Published 2013-05-22
On 2013-05-22 the FDA classified a Class II recall of BBL(tm) CDC Anaerobe 5% Sheep Blood Agar by Becton Dickinson And, citing microbiological media may be contaminated with bacteria.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1334-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-03-11 |
| Published | 2013-05-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BBL(tm) CDC Anaerobe 5% Sheep Blood Agar. Used for culturing microorganisms.
Reason
Microbiological media may be contaminated with bacteria.
Identifiers
| code_info | Model number 221733: lot 2361003 with expiration date 3/14/13 |
|---|
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-1334-2013%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.