Hemofiltration Standard Pack including BC 60 Plus-T recall
Hemofiltration Standard Pack including BC 60 Plus-T 8036. Part Number: 701066990. Used in extracorporeal circulation during cardiopulmonary bypass…
Why was Hemofiltration Standard Pack including BC 60 Plus-T recalled?
55 kits were distributed after their expiration date of September 2015.
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/batch number: 3000001571 UDI code: 607567206489
- Product
- Hemofiltration Standard Pack including BC 60 Plus-T 8036. Part Number: 701066990. Used in extracorporeal circulation during cardiopulmonary bypass…
- Recalling firm
- Maquet
- Quantity
- 55 units
- Distribution
- Distributed to the states of NM, CA, and IL.
- Recall date
- February 7, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)