Exact FDA event identifier

Event 83551

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket: August 09, 2019
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: Medline Industries 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

Medline SYRINGE, PISTON,IRR TRAY,W/.9, REF DYNC2303. Sterile Piston Irrigation Syringe Tray with Saline

Z-2358-2019

Recall number: Z-2358-2019
Initiated: August 09, 2019
Classification: Class II
Status: Ongoing
Recalling firm: Medline Industries Inc
Quantity: 11962 trays

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

open packaging

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.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Samples in the identified lot were found to have incomplete or open packaging seals.

Code information

Lot Number 19CAB954

Distribution pattern

US nationwide distribution