RUSCH LASERTUBE — Class II medical device recall Z-1684-2019
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-1684-2019 |
|---|---|
| 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 | 4,312 units |
| Reason classes | device malfunction |
| Lot numbers | 15411, 15421, 15431, 15441, 15451, 15461, 15471, 15501, 16031, 16061, 16081, 16091, 16101, 16131, 16151, 16161, 16171, 16181, 16191, 16201, 16221, 16231, 16241, 16251, 16261, 16281, 16291, 16301, 16311, 16351, 16361, 16371, 16381, 16391, 16421, 16431, 16441, 16451, 16461, 16471 and 67 more |
| Model numbers | 102004 |
Product
RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0
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-1684-2019. 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.