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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77137

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

Open FDA event record

Event summary

Timeline bucket
April 13, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Pentax of America Inc

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

4 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 4

7245C, 7245C/E, 7245D Computer Digital Video System Product Usage: The 7245C, 7245C/E and 7245D are used to electronically record, display, transfer, and store digital video data of behavior related to swallowing in the pharyngeal area for medical and pedagogical applications.

Z-2742-2017
Recall number
Z-2742-2017
Initiated
April 13, 2017
Classification
Class II
Status
Terminated
Recalling firm
Pentax of America Inc
Quantity
241 units in total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

Code information

24966-06 25281-01 26060-10 26874-03 26874-06 28669-04 28671-02 28671-04 28675-04 30150-02 30150-03 30604-09 31525-03 31525-09 31526-19 32945-04 36453-10 36453-13 38476-04 38476-07 38748-101 38976-04 39444-02 39471-09 39508-151 41735-05 41735-08 41735-11 45810-14 47969-04 80397-09 80400-01 80850-02 25631-07 27406.05 28677-10 30737-12 34599-04 37836-05 4124-07 45735-03 45810-08 80910-02

Distribution pattern

Worldwide Distribution - US Nationwide

device · product 2 of 4

9310HD Digital Video Capture Modules Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of laryngeal or pharyngeal structures, and audio data, for medical and pedagogical applications.

Z-2743-2017
Recall number
Z-2743-2017
Initiated
April 13, 2017
Classification
Class II
Status
Terminated
Recalling firm
Pentax of America Inc
Quantity
241 units in total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

Code information

80847 38953-09 40156-01 40156-09 40158-15 40669-02 40669-09 40670-05 42094-05 45852-06 46800-05 47452-01 48653-02 48653-03 49242-02 72872-49A 80361-14 80362-01 80362-02 80365-05 80399-05 80399-09 80481-07 80841-02 80842-05 80847-06 80878-07 80879-06 80879-08 80880-01 80881-05 80883-03 80884-03 80886-06 80886-11 80886-13 80887-02 80887-08

Distribution pattern

Worldwide Distribution - US Nationwide

device · product 3 of 4

9400 Laryngeal Strobe Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of laryngeal or pharyngeal structures, and audio data, for medical and pedagogical applications.

Z-2744-2017
Recall number
Z-2744-2017
Initiated
April 13, 2017
Classification
Class II
Status
Terminated
Recalling firm
Pentax of America Inc
Quantity
241 units in total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

Code information

35865-10 35866-22 37879-10 38332-20 38935-159 40356-06 41305-16 41687-20 80002-01 80002-17 80279-12

Distribution pattern

Worldwide Distribution - US Nationwide

device · product 4 of 4

9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of laryngeal or pharyngeal structures, and audio data, for medical and pedagogical applications.

Z-2745-2017
Recall number
Z-2745-2017
Initiated
April 13, 2017
Classification
Class II
Status
Terminated
Recalling firm
Pentax of America Inc
Quantity
241 units in total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

Code information

40552 22679-05 23546-06 23546-07 24036-06 24045-03 24045-06 24045-08 24045-09 24049-01 24049-03 24049-08 24231-10 24556-01 24556-06 24965-07 25282-03 25351-06 25459-01 25459-07 25459-08 25459-09 25461-01 25461-03 25461-05 25461-07 25461-09 25466-07 25466-08 25964-01 25964-03 25964-11 25965-02 25965-05 25965-12 26035-13 26055-02 26055-13 26055-18 26056-04 26056-05 26056-08 26057-03 26057-18 26058-18 26058-20 26870-09 26871-02 26871-02 26871-03 26871-03 26871-07 26871-11 26871-12 26871-14 26871-17 26871-18 26872-05 26872-06 26872-08 26872-10 26872-16 26872-18 26872-18 26872-20 26873-10 26873-16 26873-20 28073-02 28668-11 28670-03 28670-07 28670-12 28670-14 28672-14 28672-18 28674-03 28674-17 28676-08 29880-09 30001-02 30598-04 30598-09 30598-21 30599-04 30599-06 30599-13 30600-02 30600-03 30600-06 30601-11 30601-14 31523-07 31523-15 31523-21 31524-01 33226 33226-05 33226-06 33226-16 33413-05 33413-10 34162-07 34162-09 34162-20 34593-07 35263-06 35263-10 36135-14 36315-02 36315-13 36315-19 36600-13 36890-11 36890-12 36890-19 37419-13 37835-15 38524-09 38776-05 38850-01 38850-04 38850-06 39951-05 39952-024 39952-03 39952-04 41241-10 41577-09 41577-19 41577-20 41577-21 41861-14 41861-15 41861-16 42024-08 441046-01 45770-03 94965-03 48029-01 48029-06

Distribution pattern

Worldwide Distribution - US Nationwide