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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 69642

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

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Event summary

Timeline bucket
October 27, 2014
Product types
Device
Classifications
Class III
Statuses
Terminated
Recalling firm wording
CooperSurgical, 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

Cooper Surgical CANNULA-CURETTE 12MM; Model Number: MX562 The CooperSurgical SUCTION CANNULA-CURETTE device is used to remove tissue from within the uterine cavity on an outpatient basis. The primary uses for this device are for endometrial sampling especially of those patients with a higher risk of cancer. The curettes must be used with a suction pump, as well as sterile tubing, and a swivel handle. The rigid plastic suction curette is sterile and disposable. The Cannula Curette is available in the following styles: Long Curved, Long Straight, and Short Curved.

Z-0488-2015
Recall number
Z-0488-2015
Initiated
October 27, 2014
Classification
Class III
Status
Terminated
Recalling firm
CooperSurgical, Inc.
Quantity
30

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product has been identified to contain an incorrect curette type.

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

The product has been identified to contain an incorrect curette type.

Code information

Lot Code: 147234

Distribution pattern

US Distribution including the states of NY, MO and NV.