Recall events
/
Event 90196
Event summary
Timeline bucket May 11, 2022
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording MEDLINE INDUSTRIES, LP - Northfield
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
1 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 1
Medline Pill Splitters; 1 each/box; 144 boxes/carton
Z-1287-2022
Recall number Z-1287-2022
Initiated May 11, 2022
Classification Class II
Status Ongoing
Quantity 840,087 each
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process change control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1287-2022
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9357]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.
Code information Model Number: NON135000; UDI/DI:8019673489; Lot Numbers: 50920060001, 50920080001, 50920110001, 50921030001, 50921040001, 50921050001, 50921060001, 50921080001, 50921090001, 50921100001, 50921110001, 50921120001, 50922020001
Distribution pattern Worldwide distribution - US Nationwide and the countries of Canada, Singapore, Panama, and Hongkong.
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[7507]
FDA event record
· Exact recall-number query on openFDA