Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
Reported: March 7, 2018 Initiated: January 10, 2017 #Z-0705-2018
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.
Details
- Recalling Firm
- Teleflex Medical
- Units Affected
- 2140 units
- Distribution
- US only
- Location
- Research Triangle Park, NC
Frequently Asked Questions
What product was recalled? ▼
Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.. Recalled by Teleflex Medical. Units affected: 2140 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 7, 2018. Severity: Moderate. Recall number: Z-0705-2018.
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