FDA recall record

Pentax of Video Cytoscopes recall — FDA Z-2325-2017

This field action serves to retrospectively document the actions that were taken by Pentax to correct the loose suction arms on eleven (11) models of…

Class IIclassification
Z-2325-2017official record ID
Jun 21, 2017report date

Recall record at a glance

Official recordZ-2325-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPentax of America Inc.
Report dateJun 21, 2017
Recall initiation dateJan 11, 2011
Quantity1,349 - (Total - US) and 352 (Total - OUS)
LocationMontvale, NJ, United States

Official product description

Video Cytoscopes

Why the product was recalled

This field action serves to retrospectively document the actions that were taken by Pentax to correct the loose suction arms on eleven (11) models of endoscopes and to notify FDA of these actions taken in 2010-2011.

Distribution information

US Nationwide and Internationally

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.

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During endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endoscope, the observed image can become reddish or dark. Users have observed smoke…

Class IIFDA: OngoingPentax of America Inc.