RUSCH — Class II medical device recall Z-2130-2014
Terminated recall by Teleflex Medical, reported 2014-08-06, distributed nationwide. There is a possibility the handle of the laryngoscope may heat up and melt the end cap.
| Recall number | Z-2130-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Durham, NC, United States |
| Recall initiated | 2014-06-30 |
| Classified | 2014-07-29 |
| Reported by FDA | 2014-08-06 |
| Terminated | 2017-03-21 |
| Distributed | Nationwide (US) |
| Quantity | 6,246 units |
| Lot numbers | 1306522, 1306532, 1306592, 1306602, 1306612, 1306622, 1306632, 1306642, 1308522, 1308532, 1308542, 1308592, 1308602, 1308612, 1308622, 1308642, 1309542, 1309592, 1309622, 1309642, 1310522, 1310532, 1310602, 1310612, 1310622, 1310632, 1312592, 1401592, 306542 |
Product
RUSCH, TruLite, One-Piece Disposable Laryngoscope Handle Blade Combination, Non-Sterile, Rx Only, Distributed by: Teleflex Medical.
Reason for recall
There is a possibility the handle of the laryngoscope may heat up and melt the end cap.
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-2130-2014. 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.