Reported Feb 11, 2026 · Ongoing
Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 2. 25GA Laser Probe Curved Cat No. VS0120.25 3. 25GA Laser…
Vortex Surgical 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: Vortex Surgical Inc. · 4 Research Park Dr Ste 124 · Saint Charles, MO · 63304-5639
Is this the product you have?
6 of 6 products
| Model / number | Product as published |
|---|---|
VS0120.23 | 23GA Laser Probe Curved |
VS0120.25 | 25GA Laser Probe Curved |
VS0130.25 | 25GA Laser Probe Flex-Tip |
VS0125.25B | 25GA Laser Probe Illuminated Curved |
VS0140.25 | 25GA Laser Probe MaxReach |
VS0110.25 | 25GA Laser Probe Straight |
- Lot codes and dates
6 of 6 products
Products covered by this recall # Barcodes Product as published 1 81012348003681012348018023GA Laser Probe Curved Pouch UDI 810123480036 Box UDI 810123480180 Lot 2411027 2 81012348004381012348019725GA Laser Probe Curved Pouch UDI 810123480043 Box UDI 810123480197 Lot 2411026 3 81012348011181012348026525GA Laser Probe Flex-Tip Pouch UDI 810123480111 Box UDI 810123480265 Lot 2411024 2411031 4 81012348009881012348024125GA Laser Probe Illuminated Curved Pouch UDI 810123480098 Box UDI 810123480241 Lot 2411025 5 81012348013581012348028925GA Laser Probe MaxReach Pouch UDI 810123480135 Box UDI 810123480289 Lot 2410029 2411023 6 81012348001281012348016625GA Laser Probe Straight Pouch UDI 810123480012 Box UDI 810123480166 Lot 2411030 - Amount recalled
- 14,789 (8651 US; 6138 OUS)
This recall covers 13 products
The agency filed one notice per product. You are reading one of them; the other 12 are below.
Where it was sold
Why it was recalled
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.
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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