Drug recall
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006
FDA recall event 99704 · Class II · Steris Corporation
Key facts
| Event ID | 99704 |
|---|---|
| Recall numbers | Z-0070-2027, Z-0071-2027, Z-0072-2027, Z-0073-2027, Z-0074-2027, Z-0075-2027 |
| Recalling firm | Steris Corporation |
| Product type | Devices |
| Products | VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006, VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007, VERIFY Biological Steam Test Pack Model/Catalog Number: S3065, VERIFY Biological Steam Test Pack Model/Catalog Number: S3069, VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060 and 1 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the… |
| Initiation date | Aug 31, 2026 |
| Report date | Oct 14, 2026 |
| City | Mentor |
| State | OH |
| Country | United States |
| FEI number | 1527821 |
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: