RecallDepth

STERRAD NX Sterilizer Hydrogen Peroxide Gas Plasma Sterilizer Product Code 10133. The STERRAD Sterilization System is a low-temperature general-purpose sterilizer used to sterilize heat and moisture sensitive reusable medical devices.

This recall has been terminated (originally issued January 11, 2012).

Company
Advanced Sterilization Products
Recall Initiated
December 10, 2008
Posted
January 11, 2012
Terminated
December 16, 2011
Recall Number
Z-0468-2012
Quantity
776 cases
Firm Location
Irvine, CA
Official Source
View on FDA website ↗

Reason for Recall

Advanced Sterilization Products (ASP) has discovered a defect in the barcode labeling of the STERRAD NX System Cassettes 10133, Lot #08I032. This is the only lot number affected by this action. The barcodes for Lot #08I032 were printed improperly and are not capable of being read by the STERRAD unit.

Distribution

Nationwide Distribution.

Lot / Code Info

Product Code 10133; Lot #081032

Root Cause

Error in labeling

Action Taken

Advance Sterilization Products sent an "URGENT: PRODUCT RECALL" letter dated December 10, 2008 to all affected customers. The letter described the product, problem, and the actions to be taken by the customers. The letter instructs customers to examine inventory and return all sealed cassettes, using an enclosed prepaid UPS return label to: Stericycle, 2670 Executive Drive Suite A, Indianapolis, IN 46241. Additionally, a Business Reply Card and packing slip were included with the letter for customers to complete and return. Questions or further assistance was directed to ASP Customer Care Center at 888-783-7723, option 2.

More recalls by Advanced Sterilization Products

View all recalls by this company →