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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 80925

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

Open FDA event record

Event summary

Timeline bucket
August 08, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Olympus Corporation of the Americas

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

30 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 30

Bronchovideoscope BF-160

Z-3283-2018
Recall number
Z-3283-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
3948

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 2 of 30

Bronchofiberscope F-1T160

Z-3284-2018
Recall number
Z-3284-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
3317

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 3 of 30

Bronchovideoscope BF-1T180

Z-3285-2018
Recall number
Z-3285-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
5810

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 4 of 30

Bronchovidescope BF-1T240

Z-3286-2018
Recall number
Z-3286-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
1605

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 5 of 30

Bronchovideoscope BF-1T60

Z-3287-2018
Recall number
Z-3287-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
2803

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 6 of 30

Bronchovideoscope F-1TQ180

Z-3288-2018
Recall number
Z-3288-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
1134

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 7 of 30

Bronchovideoscope BF-240

Z-3289-2018
Recall number
Z-3289-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
1467

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 8 of 30

Bronchovideoscope BF-3C160

Z-3290-2018
Recall number
Z-3290-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
2318

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 9 of 30

Bronchovideoscope BF-3C40

Z-3291-2018
Recall number
Z-3291-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
2479

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 10 of 30

Bronchofiberscope BF-40

Z-3292-2018
Recall number
Z-3292-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
1347

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 11 of 30

Bronchofibercope BF-6C240

Z-3293-2018
Recall number
Z-3293-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
197

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 12 of 30

Bronchovideoscope BF-MP160F

Z-3294-2018
Recall number
Z-3294-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
672

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 13 of 30

Bronchovideoscope BF-MP60

Z-3295-2018
Recall number
Z-3295-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
653

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 14 of 30

Bronchovideoscope BF-P160

Z-3296-2018
Recall number
Z-3296-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
1874

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 15 of 30

Bronchovideoscope BF-P180

Z-3297-2018
Recall number
Z-3297-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
3705

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 16 of 30

Bronchovideoscope BF-P240

Z-3298-2018
Recall number
Z-3298-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
2163

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 17 of 30

Bronchofiberscope BF-P40

Z-3299-2018
Recall number
Z-3299-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
5607

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 18 of 30

Bronchofiberscope BF-P60

Z-3300-2018
Recall number
Z-3300-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
5545

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 19 of 30

Bronchovideoscope BF-Q180

Z-3301-2018
Recall number
Z-3301-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
5845

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 20 of 30

Bronchovideoscope BF-Q180-AC

Z-3302-2018
Recall number
Z-3302-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
655

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 21 of 30

Ultrasonic Bronchoscope BF-UC160F-OL8

Z-3303-2018
Recall number
Z-3303-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
879

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 22 of 30

Ultrasonic Bronchoscope BF-UC180F

Z-3304-2018
Recall number
Z-3304-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
4785

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 23 of 30

Bronchovideoscope BF-XP160F

Z-3305-2018
Recall number
Z-3305-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
1461

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 24 of 30

Bronchofiberscope BF-XP40

Z-3306-2018
Recall number
Z-3306-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
817

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 25 of 30

Bronchofiberscope BF-XP60

Z-3307-2018
Recall number
Z-3307-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
1296

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 26 of 30

Bronchovideoscope BF-XT160

Z-3308-2018
Recall number
Z-3308-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
861

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 27 of 30

Bronchofiberscope BF-XT40

Z-3309-2018
Recall number
Z-3309-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
931

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 28 of 30

Rhino Laryngo scope ENF-VT2

Z-3310-2018
Recall number
Z-3310-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
3701

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 29 of 30

Airway Mobilescope MAF-TM

Z-3311-2018
Recall number
Z-3311-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
3456

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.

device · product 30 of 30

Bronchovideoscope BF-1T40

Z-3312-2018
Recall number
Z-3312-2018
Initiated
August 08, 2018
Classification
Class II
Status
Terminated
Quantity
3,041

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

Code information

all lot codes

Distribution pattern

The products were distributed US nationwide and Canada.