Class II — Becton Dickinson & Co.
| Recalling firm | Becton Dickinson and Company |
|---|---|
| Registered facility | View this company's 36 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | PrepStain system rack setting was incorrectly entered on one PrepStain system during a routine preventive maintenance visit by a BD Field Service Representative. |
| Product | PrepStain Tecan US-I. For use in the screening and detection of cervical cancer. |
| Quantity | 890 instruments |
| Distribution | Worldwide Distribution-USA (nationwide) and Puerto Rico and the country of Canada. |
| Initiated | 2013-07-08 |
| Classified | 2013-08-28 |
| Terminated | 2014-05-01 |
| Recall number | Z-2111-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Becton Dickinson & Co. (Z-2111-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65779/
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