Recall Z-1371-2013— Nephron Pharmaceuticals Corp.
Class I · Terminated
Class I FDA medical device recall by Nephron Pharmaceuticals Corp., initiated 2013-04-30, terminated 2016-06-28. FDA's recall record names no specific 510(k) clearance for this event. Product: EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.. Reason: Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard..
- Recalling firm
- Nephron Pharmaceuticals Corp.
- Classification
- Class I
- Status
- Terminated
- Initiated
- 2013-04-30
- Terminated
- 2016-06-28
- Firm location
- Orlando, FL, United States
Product description
EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.
Reason for recall
Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard.
Data sourced from openFDA. This site is unofficial and independent of the FDA.