Access Hi-Low Exam Tables — Class II medical device recall Z-2531-2018
Terminated recall by Brewer Company, LLC, reported 2018-08-01, distributed in IL, MN, TX, WI. One lot, the wire harness was over-crimped on some of the connectors that go to the two vertical side switches
| Recall number | Z-2531-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Brewer Company, LLC, Menomonee Falls, WI, United States |
| Recall initiated | 2018-03-29 |
| Classified | 2018-07-24 |
| Reported by FDA | 2018-08-01 |
| Terminated | 2019-08-29 |
| Distributed | IL, MN, TX, WI |
| Quantity | 7 devices |
| Serial numbers | HL018786, HL018787, HL018788, HL018789, HL018790, HL018791, HL018797, HL018805 |
| Model numbers | 6501-XX |
Product
Access Hi-Low Exam Tables, Model 6501-XX
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2531-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.