Brewer Company, LLC: Medical Device Recall in 2018 - (Recall #: Z-2531-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Access Hi-Low Exam Tables, Model 6501-XX

Product Classification:

Class II

Date Initiated: March 29, 2018

Date Posted: August 1, 2018

Recall Number: Z-2531-2018

Event ID: 80164

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.

Status: Terminated

Product Quantity: 7 devices

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.

Voluntary or Mandated:

Voluntary: Firm initiated