Kit w/3 Ext Sets recall
Kit w/3 Ext Sets, 3 Drop-In MicroClave¿ Clear. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the…
Why was Kit w/3 Ext Sets recalled?
The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.
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 No. 3320753. Item No. 011-AM6123
- Product
- Kit w/3 Ext Sets, 3 Drop-In MicroClave¿ Clear. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the…
- Recalling firm
- ICU Medical, Inc.
- Quantity
- 100 units
- Distribution
- Distribution to Italy and France, and the following states in the US: AZ, OH, TX, WA.
- Recall date
- July 19, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)