RecallDepth

Tyvek Self-Seal Pouch with STERRAD Chemical Indicator 12332. Intended to be used to contain medical devices that are being terminally sterilized in STERRAD Sterilization Systems.

This recall has been terminated (originally issued February 22, 2011).

Company
Advanced Sterilization Products
Recall Initiated
June 23, 2010
Posted
February 22, 2011
Terminated
March 14, 2012
Recall Number
Z-1393-2011
Quantity
470
Firm Location
Irvine, CA
Official Source
View on FDA website ↗

Reason for Recall

The recall was initiated after Advanced Sterilization Products (ASP) discovered a non-conforming lot. The misaligned perforations may have caused the seal to be incomplete on some of the pouches, creating a potential breach for pouches being used to store sterilized equipment on shelves.

Distribution

Worldwide Distribution -- USA, Argentina, Australia, Canada, Chile, Czech Republic, Hong Kong, India, Japan, Panama, Peru and Puerto Rico.

Lot / Code Info

Lot Number: 2020

Root Cause

Process control

Action Taken

Advanced Sterilization Products (ASP) released Urgent: Product Recall notifications to its consignees identifying the affected product and explaining the reason for recall. The letter also discussed the impact of using this affected product and return instructions. The firm asked customers to examine their inventory, discontinue use of Tyvek Self-Seal Pouch with STERRAD Chemical Indicator 12332 and to return all unused affected products to Stericycle. Customers are to complete the Business Reply Card and return it to Stericycle.

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