MOOG Curlin Infusion Administration Set recall: Particulate Matter
MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Needleless Injection Port (Positive…
Why was MOOG Curlin Infusion Administration Set recalled?
Particulate found on the Curlin spike.
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?
UDI 38148440000488, Lot/serial numbers: CF1519507, CF1522502, CF1524406, and CF1528008.
- Product
- MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Needleless Injection Port (Positive…
- Recalling firm
- Zevex Incorporated (dba Moog Medical Medical Devices Group)
- Quantity
- 756/20-administration set cases
- Distribution
- Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.
- Recall date
- March 7, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)