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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 84725

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

Open FDA event record

Event summary

Timeline bucket
January 13, 2020
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
CooperVision 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

2 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 2

Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (extended wear)

Z-1227-2020
Recall number
Z-1227-2020
Initiated
January 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
CooperVision Inc.
Quantity
216 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrect power of lenses than the expected

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

Incorrect power of lenses than the expected

Code information

Lot Numbers: 15627000009010 15627050004010 16656000008010

Distribution pattern

US Nationwide Distribution

device · product 2 of 2

Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophilic) Contact Lens (extended wear)

Z-1228-2020
Recall number
Z-1228-2020
Initiated
January 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
CooperVision Inc.
Quantity
24

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrect power of lenses than the expected

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

Incorrect power of lenses than the expected

Code information

Lot Numbers: 15628000006509 15628000007509

Distribution pattern

US Nationwide Distribution