Pilling Aortic Punch recall: Sterility Concern
Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
Why was Pilling Aortic Punch recalled?
There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.
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 74B1500674
- Product
- Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
- Recalling firm
- TELEFLEX MEDICAL INC
- Quantity
- 1764 units
- Distribution
- Worldwide
- Recall date
- February 26, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)