Trumpet — Class II medical device recall Z-1460-2024
Ongoing recall by Technicality Inc., reported 2024-04-10, distributed nationwide. The Ring on the Trump Needle Guide can detach when excessive pressure is applied.
| Recall number | Z-1460-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Technicality Inc., Addison, IL, United States |
| Recall initiated | 2024-01-31 |
| Classified | 2024-04-02 |
| Reported by FDA | 2024-04-10 |
| Distributed | Nationwide (US) |
| Quantity | 20,000 units |
| Reason classes | device malfunction |
| Lot numbers | 22190, 22497 |
| Model numbers | TMS-200 |
Product
Trumpet, Needle Guide, Cat# TMS-200
Reason for recall
The Ring on the Trump Needle Guide can detach when excessive pressure is applied.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1460-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.