Recall Z-1373-2013— 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 Medication Cup. 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 Medication Cup. 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.