FDA recall record

Xeridiem Mediem Medical Devices EndoVive 3s Low Profile Balloon Kits Part Number: M00549550 recall — FDA Z-0987-2016

A feeding (reflux) valve leakage issue. The feeding valve appears to close inconsistently, or close in a delayed manner, when an extension set is…

Class IIclassification
Z-0987-2016official record ID
Mar 2, 2016report date

Recall record at a glance

Official recordZ-0987-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmXeridiem Mediem Medical Devices Inc.
Report dateMar 2, 2016
Recall initiation dateDec 23, 2015
Quantity38
LocationTucson, AZ, United States

Official product description

EndoVive 3s Low Profile Balloon Kits Part Number: M00549550 (XMD P/N 70-0050-B24) The EndoVive 3s Low Profile Balloon is intended to provide gastric access through a gastrointestinal stoma tract for enteral feeding, medication administration and gastric decompression. The EndoVive 3s Low Profile Balloon is indicated for use in adult and pediatric patients who require long-term feeding, are unable to tolerate oral feeding, are at low risk for aspiration or require gastric decompression and/or medication delivery directly into the stomach.

Why the product was recalled

A feeding (reflux) valve leakage issue. The feeding valve appears to close inconsistently, or close in a delayed manner, when an extension set is disconnected from the Low Profile Balloon device, thus allowing feeding solution or gastric contents to leak out of the device in some instances.

Distribution information

Nationwide distribution to MA only.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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