Reported Nov 5, 2025 · Ongoing
Brand Name
Alcon Research LLC
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: Alcon Research LLC · 6201 South Fwy · Fort Worth, TX · 76134-2099
Is this the product you have?
Brand Name
3 of 3 products
| Model / number | Product as published |
|---|---|
ENDOILLUMATOR,RFID,23G | VFC 8065750972 |
ENDOILLUMINATOR,RFID,25G | AUTO GAS FILL PAK 8065751441 |
CHANDELIER,25GA,W/RFID | 8065751577 |
- Lot codes and dates
- Catalog Number8065750918
- UDI-DI code00380657509188
- Lot/Batch Number1790L4
- Catalog Number8065750957
- UDI-DI code00380657509577
- Lot/Batch Numbers
1788D31788DC1788D11790T0179LNP179LNT179LNV179LP2179LPA17A0P817A0PC17A0PH17C12517CJEW17CXT317D0RY17DL3Y17DL4017DL4117DL4217DL4617DPRT17DPRU17ERNK17F2NR17F55K
- Catalog Number8065750972
- UDI-DI code00380657509720
- Lot/Batch Numbers17C8T2 17C8T4 17E0TX
- Catalog Number8065751014
- UDI-DI code00380657510146
- Lot/Batch Numbers
1789PV1789PW1788DD1788DE17C2MY17C2NE17DL3P17DL3U17DL3W17DL3X17E0WU17E0X017F4D6
- Catalog Number8065751441
- UDI-DI code00380657514410
- Lot/Batch Numbers17C6U5 17C359 17C35A
- Catalog Number8065751577
- UDI-DI code00380657515776
- Lot/Batch Numbers
1789P41789P51789P6179MCD17C2RV17C2RY17C2T317DPN717DPN8
- Amount recalled
- 25,778
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
Due to incomplete seals in the pouch which provide the sterile barrier.
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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