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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66832

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

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Event summary

Timeline bucket
October 29, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Kimberly-Clark 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

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

Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by Kimberly-Clark,Product code PMF22-100-10 The product is used to create lesions in nervous tissue when used with the Kimberly-Clark radiofrequency generator and probes.

Z-0850-2014
Recall number
Z-0850-2014
Initiated
October 29, 2013
Classification
Class II
Status
Terminated
Quantity
55 cases (10 units per case = 550 units)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.

Code information

Lot M3085K301 and M2327K301

Distribution pattern

US Distribution in states of: AZ, CA, DE, FL, LA, MD, MA, NJ, NY, OH, PA and TX.