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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82667

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

Open FDA event record

Event summary

Timeline bucket
March 29, 2019
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Centurion Medical Products Corporation

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

Sterile Nail Clipper Concave Edge (67710)

Z-1719-2019
Recall number
Z-1719-2019
Initiated
March 29, 2019
Classification
Class II
Status
Terminated
Quantity
Unavailable

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Compromised seal on the sterile barrier

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Compromised seal on the sterile barrier pouch.

Code information

Lot 2018120701, exp 2023-11-30

Distribution pattern

US nationwide distribution.

device · product 2 of 2

Sterile Nail Nipper, Barrel Spring (I68400), Sterile

Z-1720-2019
Recall number
Z-1720-2019
Initiated
March 29, 2019
Classification
Class II
Status
Terminated
Quantity
Unavailable

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Compromised seal on the sterile barrier

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Compromised seal on the sterile barrier pouch.

Code information

Lot 2018121101, exp 2023-11-30

Distribution pattern

US nationwide distribution.