Summary
The FDA issued a Class II for UroPass Ureteral Access Sheaths, 5 pieces/box by Olympus Corporation of the Americas. Reason: Dilator tips may break in the package and in patients during surgical procedures..
Details
Source
Device Recall
External ID
Z-2401-2023
Action Date
2023-08-23
Status
Ongoing
Category
device
Product Description
UroPass Ureteral Access Sheaths, 5 pieces/box
Lot/Code Info: Models: 61024BX, 61038BX, 61046BX, 61054BX, 61124BX, 61138BX, 61146BX, 61154BX, 61224BX, 61238BX, 61246BX, 61254BX, 61324BX, 61338BX, 61346BX, 61354BX Lots: All products manufactured in 2018 and 2019. Manufacturing date is printed on pouch label in YYYY-MM-DD format.
Quantity Affected: 9520 eaches
Reason for Recall
Dilator tips may break in the package and in patients during surgical procedures.
Distribution
Worldwide distribution - United States Nationwide and the countries of South Korea, Canada, Australia, Taiwan, Hong Kong, Japan, and Germany.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-19
Company
Center Valley, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 162 device recalls issued in the same week, part of 413 device-related FDA actions this month.
Olympus Corporation of the Americas has 334 FDA actions in our database, including 334 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Olympus Corporation of the Americas) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Olympus Corporation of the Americas have FDA actions?
Olympus Corporation of the Americas has 334 FDA actions in our database, including 334 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-2401-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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