Class I — Nurse Assist, Inc
| Recalling firm | Nurse Assist, LLC |
|---|---|
| Registered facility | NURSE ASSIST, LLC (the firm's only registered facility) |
| Classification | Class I |
| Status | Terminated |
| Reason | Potential contamination with B. cepacia. |
| Product | Normal Saline Flush 0.9% USP Sodium Chloride Injection Syringe, 3 ml fill, 5 ml fill and 10 ml fill. Product codes: 1203, 1205, 1210, 1210-BP Product usage: Saline flush |
| Quantity | 386,175 syringes |
| Distribution | Worldwide Distribution - US (Nationwide), St. Thomas, US Virgin Islands, and Internationally to Canada. |
| Initiated | 2016-10-04 |
| Classified | 2017-01-03 |
| Terminated | 2017-08-16 |
| Recall number | Z-0926-2017 |
| 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 I recall — Nurse Assist, Inc (Z-0926-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/75348/
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