Kit Model #650301018 recall: Sterility Concern
Kit Model #650301018, MTO Vascular Surgery - Cleveland Clinic PG - Product Usage: NAMIC Cath Lab and Interventional Radiology (IR) Kits consist of any…
Why was Kit Model #650301018 recalled?
Non-sterile kits intended to be sterilized prior to use were sold to accounts without sterilization capabilities.
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 5554524, Exp 12/31/2022; second lot with no lot recorded and no exp identified
- Product
- Kit Model #650301018, MTO Vascular Surgery - Cleveland Clinic PG - Product Usage: NAMIC Cath Lab and Interventional Radiology (IR) Kits consist of any…
- Recalling firm
- Medline Industries Inc
- Quantity
- 80 kits
- Distribution
- US Nationwide distribution including in the states of CA, CO, CT, OH, TX, and NY.
- Recall date
- October 14, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)