Pinook-Usa: Medical Device Recall in 2013 - (Recall #: Z-0177-2014)

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:

Pinook Micro Massager Distributed by www.pinookusa.com Used to strengthen the abdominal muscles.

Product Classification:

Class II

Date Initiated: May 23, 2013

Date Posted: November 13, 2013

Recall Number: Z-0177-2014

Event ID: 66191

Reason for Recall:

Failure to submit a premarket submission and gain approval of a medical device.

Status: Terminated

Product Quantity: 28,994 units (Micro and Mini)

Code Information:

ALL LOTS

Distribution Pattern:

Worldwide Distribution-USA (nationwide) including Puerto Rico and Guam and the states of AZ, CA, CO, FL, IL, MA, MD, MO, MT, NC, ND, NJ, NV, NY, TX, VA, and WA and the country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated