Custom Tubing Packs Custom tubing pack for oxygenators recall: Endotoxin
Custom Tubing Packs Custom tubing pack for oxygenators
Why was Custom Tubing Packs Custom tubing pack for oxygenators recalled?
Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the potential risk of exposure to endotoxin for various products.
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?
containing products included in this action which include the following serial numbers; T xxxxx, TOP xxxxx, BE-TOP xxxxx, BO-TOP xxxxx, BO-T xxxxx, BEQ-T xxxxx, and BEQ-TOP xxxxx.
- Product
- Custom Tubing Packs Custom tubing pack for oxygenators
- Recalling firm
- Maquet Cardiovascular Us Sales, Llc
- Quantity
- 72,000 units in total
- Distribution
- US Nationwide Distribution.
- Recall date
- April 20, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)