RecallDepth

Safedraw Venous Close Loop System, Blood Sampling Set, packaged in a tyvek bag, Model/Part Number 688695, Argon Critical Care Systems, Singapore Pte. Ltd., 198 Yishun Avenue 7, Singapore 768028. The blood sampling set is intended to be used for closed-loop blood sampling from the patient without the system being exposed to the outside environment.

This recall has been terminated (originally issued July 6, 2012).

Company
Argon Medical Devices, Inc
Recall Initiated
May 4, 2012
Posted
July 6, 2012
Terminated
January 14, 2013
Recall Number
Z-1946-2012
Quantity
10 pieces
Firm Location
Athens, TX
Official Source
View on FDA website ↗

Reason for Recall

Some of the kits may exhibit a potential defect with the pouch seal. The pouch issue may compromise the sterile barrier.

Distribution

Distributed only in Missouri.

Lot / Code Info

Lot Number 204889, Expiration Date March 2017

Root Cause

Packaging

Action Taken

Argon Medical Devices sent an "URGENT MEDICAL DEVICE RECALL" letter dated May 4, 2012 to all affected customers. The letter identifies the product, problem, and actions to be taken by the customers. A Recall Response Form was attached to the letter for customers to complete and return to the firm via fax to 903-577-9393. Contact the firm at CRS@argonmedical.com for questions regarding this recall.

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