Recall Z-0705-2018— Teleflex Medical
Class II · Terminated
Class II FDA medical device recall by Teleflex Medical, initiated 2017-01-10, terminated 2021-04-13. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-01-10
- Terminated
- 2021-04-13
- Firm location
- Research Triangle Park, NC, United States
Product description
Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.