RUSCH LASERTUBE — Class II medical device recall Z-1683-2019
Terminated recall by Teleflex Medical, reported 2019-06-05, distributed nationwide. The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at
| Recall number | Z-1683-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Morrisville, NC, United States |
| Recall initiated | 2019-04-01 |
| Classified | 2019-05-29 |
| Reported by FDA | 2019-06-05 |
| Terminated | 2025-06-03 |
| Distributed | Nationwide (US) |
| Quantity | 5,995 units |
| Reason classes | device malfunction |
| Lot numbers | 14141, 14151, 14161, 14171, 14201, 14211, 14231, 14261, 14271, 14281, 14291, 14301, 14311, 14361, 14431, 14441, 14451, 14461, 14471, 14481, 14491, 14501, 14511, 15041, 15051, 15071, 15081, 15091, 15101, 15111, 15121, 15131, 15161, 15191, 15201, 15211, 15221, 15231, 15241, 15251 and 106 more |
| Model numbers | 102004 |
Product
RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0
Reason for recall
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
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-1683-2019. 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.