Drug recall
INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
FDA recall event 90118 · Class II · Smith & Nephew Orthopaedics GmbH
Key facts
| Event ID | 90118 |
|---|---|
| Recall numbers | Z-1133-2022 |
| Recalling firm | Smith & Nephew Orthopaedics GmbH |
| Product type | Devices |
| Products | INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Right nails were anodized, marked, and labelled as left nails and vice versa |
| Initiation date | Apr 22, 2022 |
| Report date | Jun 1, 2022 |
| City | Tuttlingen |
| Country | Germany |
| FEI number | 3002465897 |
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: