FDAClass IINovember 13, 2013

Pinook Mini Massager recall

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

Why was Pinook Mini Massager recalled?

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

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?

ALL LOTS

Product
Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen the abdominal muscles.
Recalling firm
Pinook-Usa
Quantity
28,994 units (Mini and Micro)
Distribution
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.
Recall date
November 13, 2013
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls