FDAFDA · Food and drugs·Recall number Z-1373-2013
EZ Breathe Medication Cup. For the delivery of liquid medications for respiratory usage.
Published June 5, 2013 · Recall initiated: April 30, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Nephron Pharmaceuticals Corp.
- Distributor
- Worldwide Distribution-USA (nationwide) including DC and Puerto Rico and the states of AL, AZ, CA, CO, CT, FL, IL, IN, IO, GA, KS, KY, LA, MD, MN, MS, MO, NK, NV, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN , TX, VT, VA, WA, and WV, and the countries of Guatemala, Poland, Panama, and United Kingdom.
- Lot
- Lots #120902, Lot # 120903 and Lot # 120904
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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