FDA Device recall Z-0705-2018
Rusch Greenlite MAC 1, Catalog Number 004551001
- FDA Device
- Class II
- terminated
- Published 2018-03-07
On 2018-03-07 the FDA classified a Class II recall of Rusch Greenlite MAC 1, Catalog Number 004551001 by Teleflex Medical, citing the pouch may contain the incorrect Rusch Green Lite product size. Pouches that are labeled as containing RUSCH GREEN LITE MAC 1 may instead contain RUSCH GREEN LITE MAC 2.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0705-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-01-10 |
| Published | 2018-03-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Teleflex Medical |
| Distribution | n/a |
Product
Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
Reason
The pouch may contain the incorrect Rusch Green Lite product size. Pouches that are labeled as containing RUSCH GREEN LITE MAC 1 may instead contain RUSCH GREEN LITE MAC 2.
Identifiers
| code_info | Lot/Serial number: 1602312 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0705-2018%22
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