BD Multi Check CD4 Low Control Catalog No — Class III medical device recall Z-2233-2014
Terminated recall by BD Biosciences, Systems & Reagents, reported 2014-08-20, distributed in GA, IN, KY, MA, MD, PA, TX, VA. The outer box label contains the incorrect distribution date: Box states 2017-09-02 ; should be 2014-09-02
| Recall number | Z-2233-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | BD Biosciences, Systems & Reagents, San Jose, CA, United States |
| Recall initiated | 2014-07-18 |
| Classified | 2014-08-14 |
| Reported by FDA | 2014-08-20 |
| Terminated | 2015-05-19 |
| Distributed | GA, IN, KY, MA, MD, PA, TX, VA |
| Countries outside the US | BE, SG |
| Quantity | 85 |
| Reason classes | labeling |
| Lot numbers | BM084L |
| Model numbers | 340916 |
Product
BD Multi Check CD4 Low Control Catalog No. 340916 is intended as a complete process control for immunophenotyping by flow cytometry.
Reason for recall
The outer box label contains the incorrect distribution date: Box states 2017-09-02 ; should be 2014-09-02
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-2233-2014. 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.