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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 68281

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

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Event summary

Timeline bucket
May 06, 2014
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Beaver-Visitec International 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

Visitec Anterior Chamber Cannula, .40x22mm (27Gx7/8in) REF 585006 Cannulae are intended to irrigate and or aspirate ophthalmic solutions and liquids in or out of the eye, and remove materials where appropriate. These products are used in all sections of the eye. This cannula is a general use cannula mainly designed for the precise maintenance of optimum anterior chamber depth

Z-1664-2014
Recall number
Z-1664-2014
Initiated
May 06, 2014
Classification
Class II
Status
Terminated
Quantity
9970 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Contains a sharp tip needle when the product should contain a blunt tip cannula

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Contains a sharp tip needle when the product should contain a blunt tip cannula

Code information

Lot number: 3079324

Distribution pattern

Nationwide Distribution including AL, CT, IN, NC, NY, TX, and VA.