FDA Device recall Z-1373-2013
EZ Breathe Medication Cup
- FDA Device
- Class I
- terminated
- Published 2013-06-05
On 2013-06-05 the FDA classified a Class I recall of EZ Breathe Medication Cup by Nephron Pharmaceuticals, citing possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1373-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-04-30 |
| Published | 2013-06-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Nephron Pharmaceuticals |
| Distribution | US |
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.
Identifiers
| code_info | Lots #120902, Lot # 120903 and Lot # 120904 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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All Nephron Pharmaceuticals recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1373-2013%22
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