GOPump Elastometric infusion PumpKit with/ and without accesssories all containing Dual GOPump, part number 510076: One

FDA device recall Z-0940-2013 · posted 2013-03-13 · Terminated

Recall details

Recalling firm

Symbios Medical Products, LLC

Reason for recall

Received 2 complaints out of 458 distributed pumps in this lot, where flow restrictor bead became displaced, which were reported to permit fast flow of contents.

Action taken

Symbios sent an Urgent Medical Device Recall letter dated February 25, 2013, to all affected consignees. The letter identified the product, the problem, and the action to be taken by the consignee. Consignees were instructed to follow the enclosed 'Steps for Voluntary Field Action' in their entirety. These steps contain information about: I) identifying the product to be returned, 2) obtaining a Returned Goods Authorization number, and 3) returning the recalled product. If product(s) is (are) located, please call 317-450-0145 from 7:00 a.In '0 5:00 p.m. EDT to receive a Returned Goods Authorization umber ("RGA"). Please indicate the RGA number on the outside of the package. Attached is a Verification Form. Customers were instructed to complete and return the form even if they do not have any product to return. Their local sales representative can assist them in completing this form. Distributors of the affected product were instructed to contact Symbios at the number provided and forward the recall notice to all their affected accounts. For questions regarding this recall call 317-225-4447.

Root cause

Pending

Status

Terminated

Product code

MEB

Quantity affected

458

Distribution

Nationwide Distribution including PA, CA, OH, AL, FL, WV, TN, NJ, NC, TX, CO, NY, TX, MO, MS, SC, and GA.

Date initiated

2013-02-25

Date posted

2013-03-13

Date terminated

2014-02-13

Location

Indianapolis, IN

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