Recall events
/
Event 92779
Event summary
Timeline bucket July 27, 2023
Product types Device
Classifications Class II
Statuses Ongoing
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
15 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 15
Olympus Bronchovideoscope, Models BF-1T150, BF-1T60, BF-MP60, BF-P150, BF-P60, BF-PE2, BF-TE2, BF-XT160.
Z-2490-2023
Recall number Z-2490-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 1715 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2490-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16760]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170308185, 04953170288968, 04953170308161, 04953170339264, 04953170308277, 04953170339394, 04953170308178, 04953170288876, 04953170308123, 04953170339196, 04953170062988, 04953170339974, 04953170063008, 04953170339998, & 04953170340147; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[34186]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 15
Olympus Bronchovideoscope, Models BF-MP160F, BF-XP160F, BF-XP60.
Z-2491-2023
Recall number Z-2491-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 1072 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2491-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57480]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170340048, 04953170289064, 04953170340093, 04953170289033, 04953170340116, 04953170308154, & 04953170339240; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36095]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 15
Olympus Bronchovideoscope, Model BF-Q180-AC
Z-2492-2023
Recall number Z-2492-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 416 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2492-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16766]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170340086; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[33962]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 15
Olympus Bronchovideoscope, Models BF-1T180, BF-1TQ180, BF-P180, & BF-Q180.
Z-2493-2023
Recall number Z-2493-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 3652 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2493-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[39817]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170308215, 04953170288975, 04953170339325, 04953170308222, 04953170289002, 04953170339349, 04953170308192, 04953170317965, 04953170339288, 04953170288883, 04953170308208, 04953170288937; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[34145]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 15
Olympus Bronchovideoscope, Models BF-UC180F & BF-UC190F.
Z-2494-2023
Recall number Z-2494-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 4115 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2494-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[33890]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170356360 and 04953170399831; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36118]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 15
Olympus Airway Mobilescope, Models MAF-GM & MAF-TM.
Z-2495-2023
Recall number Z-2495-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 1859 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2495-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[10042]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170340369, 04953170288661, & 04953170288630; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36126]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 15
Olympus Bronchovideoscope, Models BF-1TH190, BF-H190, BF-Q170, & BF-Q190.
Z-2496-2023
Recall number Z-2496-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 9449 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2496-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[33886]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170335181, 04953170434778, 04953170335174, 04953170434754, 04953170342912, 04953170335198, 04953170434792; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[33973]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 15
Olympus Bronchovideoscope, Models BF-MP190F.
Z-2497-2023
Recall number Z-2497-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 441 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2497-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28501]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170395581; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36876]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 15
Olympus Bronchovideoscope, Models BF-XT190.
Z-2498-2023
Recall number Z-2498-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 235 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2498-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5029]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170402470; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36894]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2499-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 122 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2499-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[39818]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170407260, 04953170407208, and 04953170407147; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[33994]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2500-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 3949 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2500-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[33885]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170342110, 04953170434983, 04953170342134, & 04953170434990; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36720]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2501-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 2127 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2501-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[22662]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170051098, 04953170452932, & 04953170156250; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[34404]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2502-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 881 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2502-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52294]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170308130, 04953170339219, 04953170051142, & 04953170442667; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[33985]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2503-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 1004 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2503-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[10045]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170340031 & 04953170063039; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36714]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2504-2023
Initiated July 27, 2023
Classification Class II
Status Ongoing
Quantity 10801 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling Change Control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2504-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46306]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Code information UDI-DI: 04953170136856, 04953170340192, 04953170061998, 04953170340215, 04953170317576, & 04953170136825; All Serial Numbers.
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[34004]
FDA event record
· Exact recall-number query on openFDA
