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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 86699

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

Open FDA event record

Event summary

Timeline bucket
October 29, 2020
Product types
Device
Classifications
Class II
Statuses
Completed
Recalling firm wording
Chromsystems Instruments & Chemicals GmbH

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

6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva, Order No. 73039 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.

Z-0521-2021
Recall number
Z-0521-2021
Initiated
October 29, 2020
Classification
Class II
Status
Completed
Quantity
148 package units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Calibrator lots may not meet stability criteria and could result in increased results of patient samples for cortisone.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Calibrator lots may not meet stability criteria and could result in increased results of patient samples for cortisone.

Code information

Order No. 73039, Lot 3219 (expiration 08/01/2021) and Lot 1020 (Expiration 03/01/2022)

Distribution pattern

US Nationwide distribution in the states of NC and NY.

device · product 2 of 3

MassChrom Cortisol, Cortisone Saliva Control Level I, Order No. 0349 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.

Z-0522-2021
Recall number
Z-0522-2021
Initiated
October 29, 2020
Classification
Class II
Status
Completed
Quantity
880 vials

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Control lots may not meet stability criteria and could result in increased results of patient samples for cortisone.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Control lots may not meet stability criteria and could result in increased results of patient samples for cortisone.

Code information

Order No. 0349, Lot No. 3219 (Expiration 08/01/2021) and Lot No. 1020 (Expiration 03/01/2022)

Distribution pattern

US Nationwide distribution in the states of NC and NY.

device · product 3 of 3

MassChrom Cortisol, Cortisone Saliva Control Level II, Order No. 0350 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.

Z-0523-2021
Recall number
Z-0523-2021
Initiated
October 29, 2020
Classification
Class II
Status
Completed
Quantity
850 vials

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Control lots may not meet stability criteria and could result in increased results of patient samples for cortisone.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Control lots may not meet stability criteria and could result in increased results of patient samples for cortisone.

Code information

Order No. 0350, Lot No. 3219 (Expiration 08/01/2021) and Lot No. 1020 (Expiration 03/01/2022)

Distribution pattern

US Nationwide distribution in the states of NC and NY.