FDA Recall Open, Classified

The "Pacifier Activated Lullaby" (PAL) System composed of three major components: 1) the PAL Player Module (aka Player Unit), 2) the PAL Pacifier Sensor, and 3) power supply. The system is designed to encourage and reinforce effective non-nutritive sucking of premature infants.

Recall: Z-0395-2016 · Initiated October 1, 2015

Recall

Recall Number
Z-0395-2016
Event Number
72436
Firm
Powers Medical Devices, LLC
FEI Number
3009199231
Product Code
HCC
Status
Open, Classified
Root Cause
No Marketing Application
Initiated
October 1, 2015
Address
1615 S Congress Ave, Ste 103, Delray Beach, FL, 33445-6326

Description

The "Pacifier Activated Lullaby" (PAL) System composed of three major components: 1) the PAL Player Module (aka Player Unit), 2) the PAL Pacifier Sensor, and 3) power supply. The system is designed to encourage and reinforce effective non-nutritive sucking of premature infants.

Reason

PAL unit has undergone significant technological changes since the previous 510(k) and labeling is not consistent with the cleared indications of the 510(k).

Action

Powers Medical Devices, LLC intends to notify customers via certified U.S. Mail and supply the updated Instruction Manual via U.S. Mail or other tracked service. Instructions to customers include: 1) destroy the previous Instruction Manual, and replace it with the new one provided, 2) attach the new product label over the existing labeling without covering up the Model # and serial # of the device, 3) certify the destruction and replacement of the Instruction Manual nd replacement of the product label to the company using the form and self-addressed stamped envelopw provided.

Distribution

Nationwide Distribution.

Quantity

Total of 128 units