The Recall Desk
HighFDA (Devices)·Z-0965-2016·Announced 2016-03-02

Xeridiem EndoVive 3s Low Profile Balloon Kits Recalled for Valve Leakage

Xeridiem is recalling 36 EndoVive 3s Low Profile Balloon Kits because the feeding valve may close inconsistently, allowing fluid to leak.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a medical device with a functional defect that poses a risk of harm (leakage of gastric contents or feeding solution), but the source text does not report any specific injuries or illnesses, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.

Plain-English summary

Xeridiem Mediem Medical Devices Inc is recalling 36 units of the EndoVive 3s Low Profile Balloon Kits (Part Number M00549380, Lot Number 930145). The recall is limited to units distributed to Massachusetts.

The recall is due to a feeding (reflux) valve leakage issue. The valve may close inconsistently or with a delay when an extension set is disconnected, which can allow feeding solution or gastric contents to leak out of the device.

These devices are intended to provide gastric access for enteral feeding, medication administration, and gastric decompression in adult and pediatric patients. Consumers and healthcare providers should stop using the affected kits and contact the manufacturer for instructions.

The recalled product

Product
EndoVive 3s Low Profile Balloon Kits Part Number: M00549380 (XMD P/N 70-0050-822) 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 End
Affected units
36

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Part Number: M00549380 (XMD P/N 70-0050-822) Lot Number: 930145

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 105 recalled by Xeridiem Mediem Medical Devices Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 105 products in this recall →