Data Foundry

Medical device recalls 2020

Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 — Class II medical device recall Z-2729-2020

Terminated recall by TELEFLEX MEDICAL INC, reported 2020-08-05, distributed nationwide. Breaking at the point of a welded joint

Recall numberZ-2729-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTELEFLEX MEDICAL INC, Morrisville, NC, United States
Recall initiated2020-07-06
Classified2020-07-28
Reported by FDA2020-08-05
Terminated2023-08-31
DistributedNationwide (US)
Quantity20,600 units
UPC / GTIN / UDI-DI14026704663115
Lot numbers1906321, 1907321, 1908321, 1909321

Product

Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Reason for recall

Breaking at the point of a welded joint

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-2729-2020. 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.