Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 95951

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
December 16, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Integra LifeSciences Corp.

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

3 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 3

CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides constant intraventricular pressure and drainage of CSF for the management of hydrocephalus.

Z-0977-2025
Recall number
Z-0977-2025
Initiated
December 16, 2024
Classification
Class II
Status
Ongoing
Quantity
132 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling Change Control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.

Code information

UDI-DI: 10381780535874. Lot Numbers: 7432470, 7434917, 7434918 and 7438322.

Distribution pattern

US Nationwide distribution in the states of FL, NC, MA, MN, OH, DC, VA, CA, WI, NE, TX, NY, MI, OR, NJ, SC, AZ, UT, RI, IN, GA, CO and the countries of Canada, Australia, New Zealand, Cyprus, Sweden, Finland, Slovenia and Great Britain.

device · product 2 of 3

CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810PL. Implantable device that provides constant intraventricular pressure and drainage of CSF for the management of hydrocephalus.

Z-0978-2025
Recall number
Z-0978-2025
Initiated
December 16, 2024
Classification
Class II
Status
Ongoing
Quantity
170 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling Change Control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.

Code information

UDI-DI: 10381780535881. Lot Numbers: 7416790, 7432471, 7434929, 7434930, 7438312 and 7438313.

Distribution pattern

US Nationwide distribution in the states of FL, NC, MA, MN, OH, DC, VA, CA, WI, NE, TX, NY, MI, OR, NJ, SC, AZ, UT, RI, IN, GA, CO and the countries of Canada, Australia, New Zealand, Cyprus, Sweden, Finland, Slovenia and Great Britain.

device · product 3 of 3

CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Number: 828820. Implantable device that provides constant intraventricular pressure and drainage of CSF for the management of hydrocephalus.

Z-0979-2025
Recall number
Z-0979-2025
Initiated
December 16, 2024
Classification
Class II
Status
Ongoing
Quantity
46 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling Change Control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.

Code information

UDI-DI: 10381780535997. Lot Number: 7415567.

Distribution pattern

US Nationwide distribution in the states of FL, NC, MA, MN, OH, DC, VA, CA, WI, NE, TX, NY, MI, OR, NJ, SC, AZ, UT, RI, IN, GA, CO and the countries of Canada, Australia, New Zealand, Cyprus, Sweden, Finland, Slovenia and Great Britain.