Karl Storz recalls injection needles for surgery due to unverified cleaning process risking patient infections. Affected models include LUER-lock, 0.8mm, REF: 26175PD.
The efficacy of the manual cleaning process cannot be assured for the affected injection needles intended for general surgery and visceral surgery, which if used, may expose the patient to a higher risk of infection.
Karl Storz recalls certain injection needles used in surgery because their cleaning process might not work properly, increasing infection risks for patients. Healthcare providers should check if they have the affected model to avoid potential infections.
The needles' cleaning process isn't reliable, which means they might not be properly sterilized. This could lead to higher infection risks for patients during surgery.
Healthcare providers using the affected injection needles for surgery are most at risk. Patients receiving procedures with these needles could face infection risks.
Check for the model LUER-lock, 0.8mm, REF: 26175PD. All lot numbers are affected. The UDI-DI code 04048551099391 identifies the product.
Identify if your needle matches the model LUER-lock, 0.8mm, REF: 26175PD with UDI-DI 04048551099391.
The recall states the cleaning process may not be reliable, so they could pose infection risks. Use only the recalled model if you have it.
Look for the model LUER-lock, 0.8mm, REF: 26175PD with UDI-DI 04048551099391. All lot numbers are affected.
The recall doesn't specify a remedy, so check with Karl Storz Endoscopy for guidance on safe handling.
We’ve drafted a message you can send Karl Storz Endoscopy to request your refund or repair — edit it as you like.
Subject: Recall Z-0573-2024 — Karl Storz Endoscopy Karl Storz Endoscopy Hello, I own a Karl Storz Endoscopy that is covered by recall Z-0573-2024 from Karl Storz Endoscopy. 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.
