Data Foundry

Medical device recalls 2016

Intubation Scope Intended to provide optical visualization of — Class II medical device recall Z-2072-2016

Terminated recall by Pentax Medical Company, reported 2016-07-06, distributed nationwide. Pentax has become aware that operational/cleaning accessories and therapeutic devices (e.g., clips, stents, ba

Recall numberZ-2072-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmPentax Medical Company, Montvale, NJ, United States
Recall initiated2016-04-06
Classified2016-06-28
Reported by FDA2016-07-06
Terminated2017-12-21
DistributedNationwide (US)
Countries outside the USDK
Quantity1,220 units
Model numbersFI-10BS, FI-10P2, FI-10RBS, FI-13BS, FI-13P, FI-13RBS, FI-16BS, FI-16RBS, FI-9BS, FI-9RBS

Product

Intubation Scope Intended to provide optical visualization of, therapeutic access to, and use to facilitate routine or difficult tracheal intubations of the Upper Airway. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Larynx and Trachea. The instrument is introduced via the mouth or the nose, as decided by the physician, when indications consistent with the need for procedure are observed in adult and pediatric patient populations.

Reason for recall

Pentax has become aware that operational/cleaning accessories and therapeutic devices (e.g., clips, stents, balloons, etc.) can become lodged in an endoscope's instrument channel.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2072-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.