Steris recalls DSD-110-HU0163 hookups that may cause improper endoscope disinfection, risking patient infection if incorrectly connected.
IFU for hookup were incorrectly reflected within hookup IFUs and online reference system, Hookup Lookup (HULU). Use of an incorrect hookup connection and/or parameter set may prevent an endoscope from being properly disinfected, which may present a risk of patient contamination or infection
Steris is recalling hookups with model DSD-110-HU0163 that could lead to improper endoscope disinfection if connected incorrectly. This poses a risk of patient contamination or infection if the hookup is not set up properly.
The hookups may have incorrect connection settings or parameters in their instructions, which can prevent endoscopes from being properly disinfected. If the hookup is not set up correctly, it could lead to patient contamination or infection.
Healthcare facilities using endoscopes with these hookups are most at risk. Patients undergoing procedures with improperly disinfected endoscopes could be exposed to infections.
Check for model DSD-110-HU0163 on the hookups. These were sold with specific lot numbers listed in the recall notice.
Verify that the hookup is connected correctly according to the updated instructions to ensure proper endoscope disinfection.
The hookups may have incorrect connection settings or parameters in their instructions, which could prevent endoscopes from being properly disinfected, risking patient contamination or infection.
Check the model number and lot numbers listed in the recall notice to confirm if your hookups are affected. Then verify connection settings to ensure proper disinfection.
The recall does not specify a fix or remedy, but you should check connection settings to ensure proper endoscope disinfection.
We’ve drafted a message you can send Steris to request your refund or repair — edit it as you like.
Subject: Recall Z-2539-2024 — Steris Steris Hello, I own a Steris that is covered by recall Z-2539-2024 from Steris. 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.
