FDA Medical Device Recalls (openFDA)
Brewer Company, LLC: Access Hi-Low Exam Tables, Model 6501-XX
- Recall number
- Z-2531-2018
- Recalling firm
- Brewer Company, LLC
- Product
- Access Hi-Low Exam Tables, Model 6501-XX
- Status
- Terminated
- Initiated
- 2018-03-29
- Posted
- not on file
- Terminated
- 2019-08-29
- Reason
- 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.
- Root cause
- Nonconforming Material/Component
- Action
- The Brewer Company notified customers, via "MEDICAL DEVICE CORRECTION" letter, on about 03/21/2018. Instructions included to cease distribution of the product, coordinate with Brewer to schedule rework of the cable in affected tables as quickly as possible, and to notify Brewer of customers if the product was further distributed to coordinate rework of those tables. Additionally secondary controls were provided that the operator must press and continually hold the foot control pedal to operate the table, the foot control includes a stop button, depressing any pedal on the foot control will stop the table's automatic movement, and the manual instructs the operator to remove any obstructions from under the exam table prior to movement. Questions can be directed to (888) 273-9371.
- Quantity
- 7 devices
- Distribution
- Devices distributed in WI, TX, MN and IL.
- Lot, serial or model codes
- Model 6501-XX, Lot/Serial No. HL018786, HL018787, HL018788, HL018789, HL018790, HL018791, HL018797, HL018805
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LGX
- Firm FEI
- 2182536
- Firm city
- Menomonee Falls
- Firm state
- WI
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28