Drug recall
ProtectIV¿ Plus Safety IV Catheter, sterile. Packaged in a pouch and than into an inner carton.
FDA recall event 81708 · Class II · Smiths Medical ASD Inc.
Key facts
| Event ID | 81708 |
|---|---|
| Recall numbers | Z-0352-2020 |
| Recalling firm | Smiths Medical ASD Inc. |
| Product type | Devices |
| Products | ProtectIV¿ Plus Safety IV Catheter, sterile. Packaged in a pouch and than into an inner carton. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Certain lots of the Model 306701 ProtectIV¿ Plus Safety IV Catheter may exhibit damage on the safety mechanism guard. |
| Initiation date | Nov 26, 2018 |
| Report date | Nov 20, 2019 |
| Termination date | May 13, 2021 |
| City | Minneapolis |
| State | MN |
| Country | United States |
| FEI number | 3012307300 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: