Rusch Greenlite MAC 1 recall
Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
Why was Rusch Greenlite MAC 1 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot/Serial number: 1602312
- Product
- Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
- Recalling firm
- Teleflex Medical
- Quantity
- 2140 units
- Distribution
- US only
- Recall date
- March 7, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)