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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 69145

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

Open FDA event record

Event summary

Timeline bucket
August 26, 2014
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Bio-Detek, 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

3 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 3

ZOLL Pro-padz Sterile Adult Multi-Function Electrodes Part number: 8900-4012 These MFE Electrodes are used in connection with ZOLL Defibrillators for Adult patients. These disposable single use MFE's are processed through Gamma Radiation to a SAL of 1 o.e per International/ National Standards, EN ISO 11137- 2:2012 and ANSI/AAMI/ISO 11137-2:2013, Method 1, for use in a sterile environment by trained medical professionals. The indications for use include defibrillation, cardioversion, external non-invasive pacing and monitoring. These MFE electrodes have a 12 month shelf life from time of manufacture.

Z-2658-2014
Recall number
Z-2658-2014
Initiated
August 26, 2014
Classification
Class II
Status
Terminated
Recalling firm
Bio-Detek, Inc.
Quantity
198 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Sterility of device is not assured

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Sterility of device is not assured

Code information

Lot Number: 2314

Distribution pattern

Worldwide Distribution - USA (nationwide) and Internationally to Australia, Canada, and Germany.

device · product 2 of 3

ZOLL Pro-padz Sterile Adult Multi-Function Electrodes ((singles) Part number: 8900-4013 These MFE Electrodes are used in connection with ZOLL Defibrillators for Adult patients. These disposable single use MFE's are processed through Gamma Radiation to a SAL of 1 o.e per International/ National Standards, EN ISO 11137- 2:2012 and ANSI/AAMI/ISO 11137-2:2013, Method 1, for use in a sterile environment by trained medical professionals. The indications for use include defibrillation, cardioversion, external non-invasive pacing and monitoring. These MFE electrodes have a 12 month shelf life from time of manufacture.

Z-2659-2014
Recall number
Z-2659-2014
Initiated
August 26, 2014
Classification
Class II
Status
Terminated
Recalling firm
Bio-Detek, Inc.
Quantity
12 each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Sterility of device is not assured

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Sterility of device is not assured

Code information

Lot Number: 2314

Distribution pattern

Worldwide Distribution - USA (nationwide) and Internationally to Australia, Canada, and Germany.

device · product 3 of 3

ZOLL Pro-padz Sterile Adult Multi-Function Electrodes with 10-ft (3 m) leadwires Part number: 8900-4052 These MFE Electrodes are used in connection with ZOLL Defibrillators for Adult patients. These disposable single use MFE's are processed through Gamma Radiation The indications for use include defibrillation, cardioversion, external non-invasive pacing and monitoring.

Z-2660-2014
Recall number
Z-2660-2014
Initiated
August 26, 2014
Classification
Class II
Status
Terminated
Recalling firm
Bio-Detek, Inc.
Quantity
100 cases =600 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Sterility of device is not assured

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Sterility of device is not assured

Code information

Lot Number: 2314

Distribution pattern

Worldwide Distribution - USA (nationwide) and Internationally to Australia, Canada, and Germany.