Reported Jan 13, 2021 · Terminated
Greffe Aorte-LF (product info is in French); Model DYNJ31877F - Product Usage: This is a type of convenience kit used…
Medline Industries 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: Medline Industries Inc · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
- Greffe Aorte-LF (product info is in French)
- Model DYNJ31877F - Product UsageThis is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries
- Lot codes and dates
- Lot 20FBW645 (Expiration02/28/2022)
- Lot 20HBM397 (Expiration02/28/2022)
- Amount recalled
- 45
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Why it was recalled
The cylindrical sponge component is not x-ray detectable.
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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