Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82017

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

Open FDA event record

Event summary

Timeline bucket
January 16, 2019
Product types
Device
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Carolina Liquid Chemistries

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

2 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 2

CAROLINA(R) LIQUID CHEMISTRIES CORP. ETHA RGT. KIT, IVD, REF ST321

Z-1252-2019
Recall number
Z-1252-2019
Initiated
January 16, 2019
Classification
Class III
Status
Terminated
Quantity
14 kits

App-derived interpretation

No assignment exists because the official recall reason is blank.

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

Unavailable

Code information

Lot 11686

Distribution pattern

NY. NH, ME, NC, TX, AR, SC, CT, IL, CA, NJ

device · product 2 of 2

CAROLINA(R) LIQUID CHEMISTRIES CORP. ETHA RGT. KIT, IVD, REF ST321

Z-1253-2019
Recall number
Z-1253-2019
Initiated
January 16, 2019
Classification
Class III
Status
Terminated
Quantity
20 kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Supplier testing showed that the absorbance rate of the Ethyl Alcohol Assay did not meet internal quality control specifications. The defective lots will not function toward the end of shelf life.

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

Supplier testing showed that the absorbance rate of the Ethyl Alcohol Assay did not meet internal quality control specifications. The defective lots will not function toward the end of shelf life.

Code information

Lot 11687

Distribution pattern

NY. NH, ME, NC, TX, AR, SC, CT, IL, CA, NJ