Atlas FDA

Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface between DSD Automated End

FDA device recall Z-2539-2024 · posted 2024-08-08 · Open, Classified

Recall details

Recalling firm
Steris Corporation
Reason for recall
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
Action taken
Steris issued Urgent Medical Device Correction letter on 7/10 via FedEx mail. Letter states reason for recall, health risk and action to take: User Action Please ensure the following steps are completed: 1.Locate and destroy your IFU(s) relative to the hookup(s) affected by this recall. 2.Complete the Medical Device Recall Response Form included with this letter. 3.Return the completed Response Form via email to: Regulatory_Compliance@STERIS.com or via fax to 440-392-8963. As you are familiar, users have the ability to update hookup and parameter set settings in the Advantage AERs to correspond with your inventory of endoscopes. For your convenience, we have included an excerpt from the Operator Manual (Advantage Plus Pass-Thru, pages 138-140, and Advantage Plus, page 72) of the instructions on how to make these updates (see Attachment A or B, as applicable). Users are reminded to report any adverse events via FDA s MedWatch Database should an event occur. We apologize for any inconvenience this matter may cause, and as always, STERIS is dedicated to supporting our products and valued Customers. If you have questions regarding this matter, please contact your local STERIS Representative or STERIS Technical Support at 800-548-4873 or 800-444-4729.
Root cause
Error in labeling
Status
Open, Classified
Product code
FEB
Quantity affected
1082
Distribution
Worldwide distribution - United States Nationwide and the countries of Canada, Belgium, Czech Republic, Denmark, Germany, Spain, Italy, Slovenia, Slovakia, Australia, Israel, Jordan, Kuwait, Namibia,
Date initiated
2024-06-13
Date posted
2024-08-08
Location
Mentor, OH

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.

Related 510(k) clearances

RecordFirmDate
MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM (K092387)Minntech Corp.2010-04-05