The Recall Desk
HighFDA (Devices)·Z-1373-2013·Announced 2013-06-05

Nephron Pharmaceuticals Recalls EZ Breathe Medication Cups Due to Choking Hazard

Nephron Pharmaceuticals is recalling EZ Breathe Medication Cups because a component may dislodge, creating a potential choking hazard.

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 risk-of-harm product (choking hazard) where injury has not yet been reported, which aligns with the High severity criteria in the rubric.

Plain-English summary

Nephron Pharmaceuticals Corp. is recalling 750 units of the EZ Breathe Medication Cup, a device used for the delivery of liquid medications for respiratory usage. The recall affects Lots #120902, #120903, and #120904.

The recall was initiated because the "Plate A" component of the device may dislodge. If this occurs, it presents a potential choking hazard to the user.

The affected products were distributed nationwide in the United States, including DC and Puerto Rico, as well as in Guatemala, Poland, Panama, and the United Kingdom. Consumers should stop using the affected medication cups and contact the manufacturer for instructions on return or replacement.

The recalled product

Product
EZ Breathe Medication Cup. For the delivery of liquid medications for respiratory usage.
Hazard
Affected units
750

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 (2)

  • Lots #120902
  • Lot # 120903 and Lot # 120904

Distribution

Distributed nationwide across the United States.

The notice also names 34 states specifically:

Part of a larger recall action

This product is one of 3 recalled by Nephron Pharmaceuticals Corp. 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 3 products in this recall →