Rusch EasyCath Kit recall
Rusch EasyCath Kit
Why was Rusch EasyCath Kit recalled?
Potential for product not to be sterile.
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?
Catalog Number ECK120, Lot Number 74C1900304, Expiration Date 03/01/2022. Catalog Number ECK125, Lot Number 74B1901676, Expiration Date 06/01/2022.
- Product
- Rusch EasyCath Kit
- Recalling firm
- Teleflex Medical
- Quantity
- 3,700 devices
- Distribution
- Nationwide distribution to CA, FL, IL, NC, NJ, OH, OK, TX.
- Recall date
- August 7, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)