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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77704

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

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Event summary

Timeline bucket
July 05, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Novo Nordisk 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

Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product Usage: The NovoPen Echo¿ is a re-usable pen injector for single patient use by diabetics for the self injection of a desired dose of insulin. The pen injector uses Penfill 3 mL cartridge of NovoLog¿, 100 units/mL (Ux100) [insulin aspart (rDNA origin) injection] and a single use detachable and disposable pen needle (supplied separately). The pen injector allows the user to dial the desired dose from 0.5 to 30 units in 0.5 increments.

Z-0206-2018
Recall number
Z-0206-2018
Initiated
July 05, 2017
Classification
Class II
Status
Terminated
Recalling firm
Novo Nordisk Inc
Quantity
16,557 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
A small number of batches may crack or break if exposed to certain chemicals, like certain cleaning agents.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

A small number of batches may crack or break if exposed to certain chemicals, like certain cleaning agents.

Code information

U.S. batch numbers: EVG1221, EVG1226, FVG7149, FVG7458, FVG8134 & FVG8135

Distribution pattern

Nationwide distribution

Field note

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