Steris Corporation 2024-08-14 Health serious FDA
Health · FDA · Recall #FDA-Z-2538-2024
Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide the… Recall
Issued August 14, 2024 · Steris Corporation
In August 2024, Steris Corporation recalled the Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide the…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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 you should do
- 1 Stop using Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide the… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Steris Corporation to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Steris Corporation
- Category
- Health
- Recall date
- August 14, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution - United States Nationwide and the countries of Canada, Belgium, Czech Republic, Denmark, Germany, Spain, Italy, Slov
- Recall number
- FDA-Z-2538-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Steris Corporation has 5 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.