Reported Nov 5, 2025 · Ongoing
Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N/A…
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?
- Brand NameAESCULAP
- Product NameREDUCING CONVERTER 10/12MM
- TO 5MM Model/Catalog NumberEK087P
- Software VersionN/A
- Product DescriptionREDUCING
- CONVERTER 10/12MM TO 5MM ComponentN/A
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published EK087P— — 04046963620059UDI-DI: 04046963620059 — Lots 52974276, 52952133, 52954633, 52959357, 52964442, 52968887, 52972214, 52977427, 52981208, 52985519, 52988828, 52992514, 52993617, 52997919, 53002094, 53004347, 53006380, 53007625, 53010869, 53013557 - Amount recalled
- 155 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
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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