Reported Feb 26, 2020 · Terminated
Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
Teleflex Medical Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: TELEFLEX MEDICAL INC · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437
Is this the product you have?
Pilling Aortic Punch4.0 mm Standard TipREF 353440
- Lot codes and dates
- Lot Number 74B1500674
- Amount recalled
- 1764 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Why it was recalled
There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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