Class II — C.R. Bard, Inc.
| Recalling firm | C. R. Bard, Inc. |
|---|---|
| Registered facility | View this company's 19 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | During an FDA inspection it was found out that the Practical Foley Catheters to be potentially nonsterile. |
| Product | Option-vf Urinary Catheter. Female use only. Latex Free. Sterile, Rx only. |
| Quantity | 274 units |
| Distribution | US Distribution to the states of : AL, CA, CO, FL, IL, IN, MA, MD, NJ, NY, OR, PA, TN, WA, and WI. |
| Initiated | 2016-07-11 |
| Classified | 2016-09-15 |
| Terminated | 2017-03-22 |
| Recall number | Z-2830-2016 |
| 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 — C.R. Bard, Inc. (Z-2830-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/74712/
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