Drug recall
ABD HYSTERECTOMY; Model/Item Number (Kit): NAMC438-07;
FDA recall event 99808 · Class II · AVID Medical, Inc.
Key facts
| Event ID | 99808 |
|---|---|
| Recall numbers | Z-0092-2027, Z-0093-2027, Z-0094-2027, Z-0095-2027, Z-0096-2027, Z-0097-2027, Z-0098-2027, Z-0099-2027, Z-0100-2027, Z-0101-2027, Z-0102-2027, Z-0103-2027 and 3 more |
| Recalling firm | AVID Medical, Inc. |
| Product type | Devices |
| Products | ABD HYSTERECTOMY; Model/Item Number (Kit): NAMC438-07;, ADULT HEART TRAY SHANDS JACKS; Model/Item Number (Kit): SHND419-08;, CRANIOTOMY PACK; Model/Item Number (Kit): WRNM035-20;, DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;, DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28; and 10 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product may be potentially contaminated with a lubricant used during the manufacturing process. |
| Initiation date | Aug 10, 2026 |
| Report date | Oct 14, 2026 |
| City | Toano |
| State | VA |
| Country | United States |
| FEI number | 1047429 |
At a glance
- 10–99 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: