Drug recall
3M Durapore Advanced, Surgical Tape, Model Numbers: 1590-0, 1590-1, 1590-2, 1590-3, 1591-0, 1591-1, 1591-2…
FDA recall event 84376 · Class II · 3M Company - Health Care Business
Key facts
| Event ID | 84376 |
|---|---|
| Recall numbers | Z-0719-2020 |
| Recalling firm | 3M Company - Health Care Business |
| Product type | Devices |
| Products | 3M Durapore Advanced, Surgical Tape, Model Numbers: 1590-0, 1590-1, 1590-2, 1590-3, 1591-0, 1591-1, 1591-2, 1591-3, 1590S-1, 1590S-2, 1590B-118, 1590B-136 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | While the product meets all safety and efficacy criteria, long term exposure of 3M Durapore Advanced Surgical Tape to continuous high moisture clinical applications has not fully met all of 3M s… |
| Initiation date | Nov 21, 2019 |
| Report date | Jan 1, 2020 |
| Termination date | Apr 23, 2021 |
| City | Saint Paul |
| State | MN |
| Country | United States |
| FEI number | 2110898 |
At a glance
- 1–9 Products in this recall
- 10–99 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: