Exact FDA event identifier

Event 80164

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

Open FDA event record

Event summary

Timeline bucket: March 29, 2018
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Brewer Company, LLC

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

Access Hi-Low Exam Tables, Model 6501-XX

Z-2531-2018

Recall number: Z-2531-2018
Initiated: March 29, 2018
Classification: Class II
Status: Terminated
Recalling firm: Brewer Company, LLC
Quantity: 7 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

One lot, the wire harness was over-crimped on some of the connectors that go to the two vertical side switches on the exam table.

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

One lot, the wire harness was over-crimped on some of the connectors that go to the two vertical side switches on the exam table.

Code information

Model 6501-XX, Lot/Serial No. HL018786, HL018787, HL018788, HL018789, HL018790, HL018791, HL018797, HL018805

Distribution pattern

Devices distributed in WI, TX, MN and IL.