Class II — Becton Dickinson & Company
| 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 | Iincorrectly packaged without the required lidocaine as labeled |
| Product | PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D |
| Quantity | 655 kits |
| Distribution | AZ, CT, GA, IL, LA, MA, MI, MN, ND, NE, NY, OH, SD, TX), |
| Initiated | 2020-03-17 |
| Classified | 2020-05-08 |
| Terminated | 2020-10-21 |
| Recall number | Z-1946-2020 |
| 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 & Company (Z-1946-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85287/
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