Exact FDA event identifier

Event 84165

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

Open FDA event record

Event summary

Timeline bucket: October 24, 2019
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Centurion Medical Products Corporation

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

Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - REG Code: DT11955

Z-0344-2020

Recall number: Z-0344-2020
Initiated: October 24, 2019
Classification: Class II
Status: Terminated
Recalling firm: Centurion Medical Products Corporation
Quantity: 80 units

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0

Sterile packaging incomplete seals may compromise

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Sterile packaging incomplete seals may compromise sterility of the product

Code information

Lot/Batch Number: 2019052190 Exp Date: 5/31/2024

Distribution pattern

Nationwide