Hex Driver Part Number HXDRIVER-2 — Class II medical device recall Z-1373-2018
Terminated recall by TriMed Inc., reported 2018-04-18. Following the completion of sterilization cycle(s) of the impacted Hex Driver, the epoxy color band on the imp
| Recall number | Z-1373-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TriMed Inc., Santa Clarita, CA, United States |
| Recall initiated | 2018-01-11 |
| Classified | 2018-04-12 |
| Reported by FDA | 2018-04-18 |
| Terminated | 2024-01-18 |
| Countries outside the US | CN |
| Quantity | 1,525 devices |
| Lot numbers | 91856, 91857, 91858, 91956, 91957, 92235, 922361, 922362, 92237, 92238, 92656 |
| Model numbers | DVHX-2.5/130CAO, HXDRIVER-2.0AO, HXDRIVER-3.5AO, HXDRIVR-2.5AO, HXDRIVR-2.5CLAO, HXDRIVR-3.0AO |
Product
Hex Driver Part Number HXDRIVER-2.0 AO; Hex Driver Part Number HXDRIVR-2.5 AO; Hex Driver Part Number HXDRIVR-2.5CL AO; Hex Driver Part Number DVHX-2.5/130C AO; Hex Driver Part Number HXDRIVR-3.0 AO; Hex Driver Part Number HXDRIVER-3.5AO
Reason for recall
Following the completion of sterilization cycle(s) of the impacted Hex Driver, the epoxy color band on the impacted Hex Driver can migrate down the shaft and/or potentially onto the sterilization tray or caddy.
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-1373-2018. 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.