Recall events
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Event 91122
Event summary
Timeline bucket October 31, 2022
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Owens & Minor Distribution, 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
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
Aero Blue Performance Surgical Gown, XL- Sterile surgical gown Code: 41734
Z-0343-2023
Recall number Z-0343-2023
Initiated October 31, 2022
Classification Class II
Status Ongoing
Quantity 72 cases (2160 pouches)
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
open seal
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0343-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9934]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential open seal pouches compromising sterility resulting in the use of a non-sterile product in surgery could lead to patient infection
Code information UDI-DI: 10680651417340 Lot Number: AH1215T51
Distribution pattern IL, IN, WV
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[6969]
FDA event record
· Exact recall-number query on openFDA