Class II — Brewer Company, LLC
| Recalling firm | The Brewer Company LLC |
|---|---|
| Registered facility | The Brewer Company LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| 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. |
| Product | Access Hi-Low Exam Tables, Model 6501-XX |
| Quantity | 7 devices |
| Distribution | Devices distributed in WI, TX, MN and IL. |
| Initiated | 2018-03-29 |
| Classified | 2018-07-24 |
| Terminated | 2019-08-29 |
| Recall number | Z-2531-2018 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Brewer Company, LLC (Z-2531-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80164/
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