Medical Device Recall: Z-0044-2014

FDA Recalls dataset · Firm: Advanced Sterilization Products · Status: Terminated

Recall Action Class: N/A Date Initiated: 2013-09-18 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0044-2014.

Recall Res Number
Z-0044-2014
Recalling Firm / Manufacturer
FEI Number
3003662624
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2013-09-18
Date Posted
2013-10-22
Date Terminated
2014-01-13
Product Code
MLR
Event Number
66317
Product Quantity
2,995 units
Product Description STERRAD 100NX Cassettes The STERRAD Sterilization System is a low temperature general purpose sterilizer used to sterilize heat and moisture sensitive reusable medical devices.

Reason for Recall Advanced Sterilization Products (ASP) is recalling the three lots (13F049, 13F050, 13F051) STERRAD 100NX Cassettes because ASP has determined that the leak indicator on the cassettes is effective for only 12 months of the cassette's labeled 15-month shelf-life.

Action Details Advanced Sterilization Products (ASP) sent an Urgent Medical Device Recall letter on September 18, 2013, to all affected customers. The letter informed the customers of the problems identified and the actions to be taken. Customers were instructed to examine their inventory and return all affected cassettes using the enclosed prepaid UPS return lave to Stericycle. Customers were asked to count their inventory and record the data on the enclosed Business Reply Card and Packing Slip. Customers were asked to provide the notice to anyone in their facility that needs to be informed. Customers were also asked to maintain a copy of the notice with the affected product. Customers with questions or suspected problems were instructed to contact Stericycle directly at 1-877-257-7119. For questions regarding this recall call 949-453-6400.

Distribution Pattern Nationwide Distribution

Code Information / Serial Numbers Lot# 13F050, 13F051, 13F049

Related Establishments / Registrations

Public Record Disclaimer

This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.

Account Required Full available specs will require a free AvaSpecs account.