SMMT ambIT Reusable Program - Luer Cass recall
SMMT ambIT Reusable Program - Luer Cass, Product Code: 220568
Why was SMMT ambIT Reusable Program - Luer Cass recalled?
Some of the ambIT kits were potentially distributed without an air in-line filter.
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 Number (Expiration Date): 30191805 (17 Jan 2025)
- Product
- SMMT ambIT Reusable Program - Luer Cass, Product Code: 220568
- Recalling firm
- Avanos Medical, Inc.
- Quantity
- 40 cases (200 cassettes)
- Distribution
- Worldwide distribution - US Nationwide distribution in the states of Texas and Oregon. The country of Australia.
- Recall date
- June 14, 2023
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)