Reported Mar 13, 2024 · Ongoing
DISP.HASSON TROCAR 12/110MM, Product Code EK240SU. For use in laparoscopic procedures.
Aesculap 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: Aesculap Inc · 3773 Corporate Pkwy · Center Valley, PA · 18034-8217
Is this the product you have?
- DISP.HASSON TROCAR 12/110MM, Product Code EK240SU. For use in laparoscopic procedures.
- Lot codes and dates
- Product CodeEK240SU
- UDI/DI04046963620493
- Batch Numbers (Expiration Date)52581648 (01/31/2025)
- Amount recalled
- 6 pieces
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
The sterile blister packaging may be damaged, and sterility may be compromised.
This product could cause temporary or reversible health problems — stop using it.
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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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