Becton — Class II medical device recall Z-0701-2013
Terminated recall by Becton Dickinson & Co., reported 2013-01-30, distributed in CT, FL, IL, KS, MD, MI, MO, NY…. Clinical diagnostic instrument may exhibit minor defects, which could lead to erroneous test results.
| Recall number | Z-0701-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Co., Sparks, MD, United States |
| Recall initiated | 2012-09-18 |
| Classified | 2013-01-22 |
| Reported by FDA | 2013-01-30 |
| Terminated | 2013-02-04 |
| Distributed | CT, FL, IL, KS, MD, MI, MO, NY, PA, RI, TX, WI |
| Countries outside the US | CA, JP |
| Quantity | 86 instruments |
| Serial numbers | CM0001, CM0105, MX0001, MX0065 |
| Model numbers | 441916 |
Product
Becton, Dickinson and Company, BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument.
Reason for recall
Clinical diagnostic instrument may exhibit minor defects, which could lead to erroneous test results.
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-0701-2013. 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.