Nephron Pharmaceuticals Corp.: Medical Device Recall in 2013 - (Recall #: Z-1373-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

EZ Breathe Medication Cup. For the delivery of liquid medications for respiratory usage.

Product Classification:

Class I

Date Initiated: April 30, 2013

Date Posted: June 5, 2013

Recall Number: Z-1373-2013

Event ID: 65070

Reason for Recall:

Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard.

Status: Terminated

Product Quantity: 750 Medications Cups

Code Information:

Lots #120902, Lot # 120903 and Lot # 120904

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated