Official recall record
Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscop
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2024-06-13
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00677964086878
- Brand on record
- Steris Corporation
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2026-09-23 · US FDA — Medical Devices
HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgi - 2026-08-31 · US FDA — Medical Devices
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007 - 2026-08-31 · US FDA — Medical Devices
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.