The Recall Desk
HighFDA (Devices)·Z-0977-2016·Announced 2016-03-02

Xeridiem EndoVive 3s Balloon Kits Recalled for Valve Leakage

Xeridiem is recalling 39 EndoVive 3s Low Profile Balloon Kits because the feeding valve may close inconsistently, allowing solution or gastric contents 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 is classified as FDA Class II. The hazard involves leakage of gastric contents or feeding solution, which presents a risk of harm (infection or aspiration) even though specific injuries are not reported in the text.

Plain-English summary

Xeridiem Mediem Medical Devices Inc is recalling 39 units of EndoVive 3s Low Profile Balloon Kits, Part Number M00548750 (XMD P/N 70-0050-A18), Lot Number 929716. The recall was initiated due to a feeding (reflux) valve leakage issue.

The defect involves the feeding valve closing inconsistently or in a delayed manner when an extension set is disconnected from the Low Profile Balloon device. This malfunction allows feeding solution or gastric contents to leak out of the device in some instances.

The affected products were distributed nationwide to Massachusetts only. No specific instructions for consumers are provided in the source text.

The recalled product

Product
EndoVive 3s Low Profile Balloon Kits Part Number: M00548750 (XMD P/N 70-0050-A18)
Affected units
39

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: M00548750 (XMD P/N 70-0050-A18) Lot Number: 929716

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 →