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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66191

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 23, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Pinook-Usa

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

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

Z-0176-2014
Recall number
Z-0176-2014
Initiated
May 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
Pinook-Usa
Quantity
28,994 units (Mini and Micro)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Failure to submit a premarket submission and gain approval of a medical device.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

No Marketing Application

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

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.

device · product 2 of 2

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

Z-0177-2014
Recall number
Z-0177-2014
Initiated
May 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
Pinook-Usa
Quantity
28,994 units (Micro and Mini)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Failure to submit a premarket submission and gain approval of a medical device.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

No Marketing Application

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

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.

Field note

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