NAMIC Fluid Delivery Set - 72" recall: Sterility Concern
NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005
Why was NAMIC Fluid Delivery Set - 72" recalled?
The product has the potential to be non-sterile as it was not packaged in accordance to specification.
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 Number: 5122528
- Product
- NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005
- Recalling firm
- Angiodynamics Inc. (Navilyst Medical Inc.)
- Quantity
- 8 boxes/25 units
- Distribution
- CA, KY, MD, OR, VA, TX
- Recall date
- April 26, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)