Drug recall
TMJ Arthroscopy Drape, 85''x 96''
FDA recall event 89956 · Class II · Microtek Medical Inc.
Key facts
| Event ID | 89956 |
|---|---|
| Recall numbers | Z-1071-2022 |
| Recalling firm | Microtek Medical Inc. |
| Product type | Devices |
| Products | TMJ Arthroscopy Drape, 85''x 96'' |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Latex content in product was labeled incorrectly as latex free. |
| Initiation date | Apr 8, 2022 |
| Report date | May 18, 2022 |
| Termination date | Jun 5, 2024 |
| City | Saint Paul |
| State | MN |
| Country | United States |
| FEI number | 3014342658 |
At a glance
- 1–9 Products in this recall
- None 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: