FDAFDA · Food and drugs·Recall number Z-1269-2020
Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
Published February 26, 2020 · Recall initiated: January 13, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- TELEFLEX MEDICAL INC
- Distributor
- Worldwide
- Lot
- Lot Number 74B1500674
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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