FDAClass IJune 5, 2013

EZ Breathe Medication Cup. For the delivery of liquid recall

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

Why was EZ Breathe Medication Cup. For the delivery of liquid recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lots #120902, Lot # 120903 and Lot # 120904

Product
EZ Breathe Medication Cup. For the delivery of liquid medications for respiratory usage.
Recalling firm
Nephron Pharmaceuticals Corp.
Quantity
750 Medications Cups
Distribution
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.
Recall date
June 5, 2013
Classification
Class I
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls