Recall Z-1336-2014— Energizer Personal Care

Name: FDA recall Z-1336-2014
Creator: U.S. Food and Drug Administration
Published: 2014-03-18

Class II · Terminated

Class II FDA medical device recall by Energizer Personal Care, initiated 2014-03-18, terminated 2016-06-10. It names one FDA 510(k) clearance: K061013. Product: Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120, which is included with the package.. Reason: Some of the power adapters outer casings may become loose and separate, resulting in a potential for electric shock..

Recalling firm: Energizer Personal Care
Classification: Class II
Status: Terminated
Initiated: 2014-03-18
Terminated: 2016-06-10
Firm location: Shelton, CT, United States

510(k) clearances named in this recall

1 on FDA's record

K061013 — PLAYTEX EMBRACE PETITE BREAST PUMPPlaytex Products, Inc.·cleared 2006-08-15

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120, which is included with the package.

Reason for recall

Some of the power adapters outer casings may become loose and separate, resulting in a potential for electric shock.

Data sourced from openFDA. This site is unofficial and independent of the FDA.