Gambro Cartridge Blood Set Prime Line recall
Gambro Cartridge Blood Set Prime Line, product code 101025 - Product Usage: intended for single use in a hemodialysis treatment using the Phoenix…
Why was Gambro Cartridge Blood Set Prime Line recalled?
complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
UDI 07332414007836, All lots within expiry
- Product
- Gambro Cartridge Blood Set Prime Line, product code 101025 - Product Usage: intended for single use in a hemodialysis treatment using the Phoenix…
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 7437480 units
- Distribution
- Worldwide distribution.
- Recall date
- February 24, 2021
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)