Z-1334-2013 Class II Terminated
FDA device recall Z-1334-2013 was initiated by Becton Dickinson & Co. on Mar 11, 2013 and is designated Class II. Reason for recall: Microbiological media may be contaminated with bacteria. The recall status is terminated (terminated Jun 24, 2013). Affected quantity: 521,160 total pieces (all three recalled products).
Recall Details
- Product Type
- Devices
- Report Date
- May 22, 2013
- Initiation Date
- Mar 11, 2013
- Termination Date
- Jun 24, 2013
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 521,160 total pieces (all three recalled products)
Product Description
BBL(tm) CDC Anaerobe 5% Sheep Blood Agar. Used for culturing microorganisms.
Reason for Recall
Microbiological media may be contaminated with bacteria.
Distribution Pattern
Worldwide Distribution-USA (nationwide) including Puerto Rico, Virgin Islands, and Guam and the countries of Columbia, Japan, Singapore, Canada, Turks, Calicos Islands.
Code Information
Model number 221733: lot 2361003 with expiration date 3/14/13
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1334-2013
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026