Recall Z-1371-2013

Nephron Pharmaceuticals Corp. · initiated April 30, 2013

Class I Terminated

Class I – dangerous or defective products that could cause serious health problems or death

Product

EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.

Codes / lots: Model # EZ-100 Lots # R2029A, R2029B, R2039A, R2042A, R2045A, and R2047A. Atomizer Serial Number Ranges: 1206034476-1206069065 1207003710-1237038299 1207046505-1207081124 1208027421-1208062155 1209000001-1209069179 1209069180-1209069202 1209069203-1209069460 1210000001-1210103680 1210104001-1210104044

Reason for recall

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

FDA-determined cause: Nonconforming Material/Component

Action taken

The firm, Nephron Pharmaceuticals Corporation, notified its consignees on April 30, 2013, and May 3, 2013, of the problem via a recall notice and a Press Release, respectively. The firm directed consignees to discontinue use of any EZ Breathe atomizer units contained in the Asthmanefrin Starter Kits with the affected lot numbers and also those that were sold individually. Customers were directed to return all affected product.

Details

Recall number
Z-1371-2013
Initiated
April 30, 2013
Posted by FDA
May 29, 2013
Terminated
June 28, 2016
Product code
CCQ – Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Quantity
604 each
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.
Recalling firm
Nephron Pharmaceuticals Corp., Orlando, FL

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-1372-2013 Class IAsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one (1) EZ Breathe…Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard. 04/30/2013Terminated
Z-1373-2013 Class IEZ Breathe Medication Cup. For the delivery of liquid medications for respiratory usage.Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard. 04/30/2013Terminated