Exact FDA event identifier

Event 93377

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

Open FDA event record

Event summary

Timeline bucket: November 03, 2023
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: Remington Medical, 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

Remington MEDICAL Drainage Bag, REF 600-D;

Z-0487-2024

Recall number: Z-0487-2024
Initiated: November 03, 2023
Classification: Class II
Status: Ongoing
Recalling firm: Remington Medical, Inc.
Quantity: 3080 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.

Code information

UDI/DI 20813079020008, Lot Number 2325111

Distribution pattern

US: PA and FL