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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 70045

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

Open FDA event record

Event summary

Timeline bucket
November 25, 2014
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Nonin Medical, 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

SenSmart, Regional Oximetry EQUANOX Classic Plus Adult/Pediatric Sensor > 40 kg., Model 8003CA (REF 9824-001, 3-Wavelength), 8004CA (REF 9705-001, 4-Wavelength), with associated materials (INT-100 cable, operator's manual; and Quick Start Guide). Sensors are single-packed in a pouch, then multi-packed, 20 per shelf-box.

Z-0901-2015
Recall number
Z-0901-2015
Initiated
November 25, 2014
Classification
Class II
Status
Terminated
Recalling firm
Nonin Medical, Inc
Quantity
5892 (5452 US, 440 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Nonin Medical is conducting a recall of certain regional oximetry sensors and associated products. They have received reports of signal loss during use of our shortcabled regional oximetry sensors with diaphoretic patients. No injury or illness have been reported.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Nonin Medical is conducting a recall of certain regional oximetry sensors and associated products. They have received reports of signal loss during use of our shortcabled regional oximetry sensors with diaphoretic patients. No injury or illness have been reported.

Code information

PRTNUM_72 PMDES1_01 LOTNUM_72 8825001 PKG ASSY, INT100 25605 8825001 PKG ASSY, INT100 414312 8825001 PKG ASSY, INT100 414353 8825001 PKG ASSY, INT100 414405 8825001 PKG ASSY, INT100 418061 9705001 PKG ASSY, 8004CA, 20PK 37245 9705001 PKG ASSY, 8004CA, 20PK 36349 9705001 PKG ASSY, 8004CA, 20PK 36475 9705001 PKG ASSY, 8004CA, 20PK 36476 9705001 PKG ASSY, 8004CA, 20PK 36477 9705001 PKG ASSY, 8004CA, 20PK 36593 9705001 PKG ASSY, 8004CA, 20PK 36693 9705001 PKG ASSY, 8004CA, 20PK 36694 9705001 PKG ASSY, 8004CA, 20PK 36695 9705001 PKG ASSY, 8004CA, 20PK 36696 9705001 PKG ASSY, 8004CA, 20PK 36697 9705001 PKG ASSY, 8004CA, 20PK 36698 9705001 PKG ASSY, 8004CA, 20PK 36886 9705001 PKG ASSY, 8004CA, 20PK 36887 9705001 PKG ASSY, 8004CA, 20PK 36989 9705001 PKG ASSY, 8004CA, 20PK 37066 9705001 PKG ASSY, 8004CA, 20PK 37094 9705001 PKG ASSY, 8004CA, 20PK 37151 9705001 PKG ASSY, 8004CA, 20PK 37245 9705001 PKG ASSY, 8004CA, 20PK 37374 9705001 PKG ASSY, 8004CA, 20PK 37410 9705001 PKG ASSY, 8004CA, 20PK 37514 9705001 PKG ASSY, 8004CA, 20PK 37515 9705001 PKG ASSY, 8004CA, 20PK 37591 9705001 PKG ASSY, 8004CA, 20PK 37607 9705001 PKG ASSY, 8004CA, 20PK 37669 9705001 PKG ASSY, 8004CA, 20PK 37670 9824001 PKG ASSY, 8003CA, 20 PK 36611 9824001 PKG ASSY, 8003CA, 20 PK 36888 9824001 PKG ASSY, 8003CA, 20 PK 36937 9824001 PKG ASSY, 8003CA, 20 PK 37090 9824001 PKG ASSY, 8003CA, 20 PK 37231 9824001 PKG ASSY, 8003CA, 20 PK 37575

Distribution pattern

To be provided later.

Field note

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