Vortex Surgical recalls VS0801B Illuminated Depressor due to potential injury risk. Affected units have specific UDI codes. Stop using immediately to avoid injury.
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Vortex Surgical is recalling their VS08:01B Illuminated Depressor device because it may cause injury. This recall affects specific units with unique UDI codes. Users should stop using the product immediately to prevent potential harm.
The device may cause injury during surgical procedures due to a potential malfunction. This risk is present in the specific units identified by the UDI codes listed in the recall.
Medical professionals using this device for surgery are most at risk. The recall applies to specific units sold with particular UDI codes.
Check for the UDI code 810123481309 on the pouch or 810123481712 on the box. The product was sold with lot number 2403027R.
Immediately stop using the Vortex Surgical TID Pharos Illuminated Depressor if you have the affected units with the specified UDI codes.
The recalled device is the Vortex Surgical TID Pharos Illuminated Depressor, model VS0801B.
Check for the UDI code 810123481309 on the pouch or 810123481712 on the box. The product was sold with lot number 2403027R.
Stop using the device immediately and contact Vortex Surgical for further instructions.
We’ve drafted a message you can send Vortex Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1254-2026 — Vortex Surgical Vortex Surgical Hello, I own a Vortex Surgical that is covered by recall Z-1254-2026 from Vortex Surgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
