RecallDepth

B. Braun Blistered Omnifix L.L. Syringe packaged in the Easypump LT 100-48, 100 ml x 2 ml/hr Used to provide an optional filling device for the Easypump.

This recall has been terminated (originally issued September 24, 2009).

Company
I-Flow Corporation
Recall Initiated
August 1, 2008
Posted
September 24, 2009
Terminated
October 7, 2009
Recall Number
Z-2249-2009
Quantity
569 units
Firm Location
Lake Forest, CA
Official Source
View on FDA website ↗

Reason for Recall

I-Flow identified a B. Braun syringe package that had a tear/hole in the paper portion of the primary package.

Distribution

France

Lot / Code Info

Lot Number: 7B2775

Root Cause

Packaging process control

Action Taken

I-Flow sent a recall letter dated August 1, 2008 to consignees telling them of the above mentioned recall and asking them to Inspect their Easypump inventory to determine if they have any of the affected lots identified on this Recall Notification Letter. They were told not to distribute affected devices and quarantined remaining inventory immediately. They were asked to check the appropriate response on the attached I-Flow Fax sheet and return the form back to I-Flow within 48 hours of receipt. The I-Flow Customer Service number (949) 206-2700, and hours of operation (7:00 am - 5:00 pm PST) were provided to answer questions.

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