Recall events
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Event 74671
Event summary
Timeline bucket July 11, 2016
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Bausch & Lomb Inc Irb
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
2 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 2
Laseredge 1.1mm Arrow Knife Angled, REF E7592 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.
Z-2365-2019
Recall number Z-2365-2019
Initiated July 11, 2016
Classification Class II
Status Terminated
Quantity 384 packs/6 blades (2,304 individual blades)
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Possible dull knife edge
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Vendor change control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2365-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27248]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Possible dull knife edge
Code information Lot Numbers: MAWS530 MAXA950 Expiry Dates: 01-2021
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[29363]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 2
Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED, REF E7599 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.
Z-2366-2019
Recall number Z-2366-2019
Initiated July 11, 2016
Classification Class II
Status Terminated
Quantity 165 packs/6 blades (990 individiual blades)
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Possible dull knife edge
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Vendor change control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2366-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3456]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Possible dull knife edge
Code information Lot Number: MAXZ170 Expiry Date: 01/28/2021
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[28670]
FDA event record
· Exact recall-number query on openFDA
