Drug recall
Convenience Kits, MOHS "OPENING" PROCEDURE TRAY
FDA recall event 73465 · Class II · Avid Medical, Inc.
Key facts
| Event ID | 73465 |
|---|---|
| Recall numbers | Z-2589-2016, Z-2590-2016, Z-2591-2016, Z-2592-2016 |
| Recalling firm | Avid Medical, Inc. |
| Product type | Devices |
| Products | Convenience Kits, MOHS "OPENING" PROCEDURE TRAY, MAMMOGRAPHY, PEDIATRIC KIDNEY BIOPSY TRAY |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as… |
| Initiation date | Oct 5, 2015 |
| Report date | Aug 24, 2016 |
| Termination date | Jan 10, 2017 |
| City | Toano |
| State | VA |
| Country | United States |
| FEI number | 1047429 |
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: