Exact FDA event identifier

Event 90962

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

Open FDA event record

Event summary

Timeline bucket: September 20, 2022
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: TELEFLEX LLC

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

Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116). Urinary catheter.

Z-0227-2023

Recall number: Z-0227-2023
Initiated: September 20, 2022
Classification: Class II
Status: Ongoing
Recalling firm: TELEFLEX LLC
Quantity: 7200 catheters

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Product may not be sterile

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product may not be sterile

Code information

UDI (01)24026704323245(17)250405(10)74E2200810

Distribution pattern

TN, CA, NC, TX, FL, OH, MO, IL, OR