Drug recall
KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS…
FDA recall event 91850 · Class II · Pro-Dex Inc
Key facts
| Event ID | 91850 |
|---|---|
| Recall numbers | Z-1391-2023 |
| Recalling firm | Pro-Dex Inc |
| Product type | Devices |
| Products | KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect Unique Device Identifier/GTIN code was used on product. |
| Initiation date | Feb 14, 2023 |
| Report date | Apr 26, 2023 |
| City | Irvine |
| State | CA |
| Country | United States |
| FEI number | 2081135 |
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: