Brewer Access Hi-Low Exam Tables Model 650: Over-crimped Wire Harness Risk

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Recalling firmBrewer Company, LLCN88 W13901 Main St, N/A · Menomonee Falls, WI 53051-2330

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Brewer is recalling Access Hi-Low Exam Tables Model 6501-XX due to a wire harness that was over-crimped on some connectors. This could lead to electrical problems if the table is used improperly. Affected units have specific lot numbers listed in the recall.

Why it’s dangerous

The wire harness was over-crimped on some connectors that connect to the vertical side switches. This could cause electrical issues if the table is moved or adjusted improperly, potentially leading to malfunction.

Who’s affected

Healthcare providers and patients using the Access Hi-Low Exam Tables Model 6501-XX are likely affected. Those with the specific lot numbers listed in the recall are at the highest risk.

How to tell if you have this one

Check the product label for the model number 6501-XX. Affected units have lot numbers HL018786 through HL018805.

Brand
Brewer
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the model number 6501-XX and lot numbers HL018786 to HL018805 on the product label.

✎ GovInfoNow

Questions people ask

What is the specific model number of the recalled tables?

The recalled model is Access Hi-Low Exam Tables Model 6501-XX.

Which lot numbers are affected?

Affected lot numbers are HL018786, HL018787, HL018788, HL018789, HL018790, HL018791, HL018797, and HL018805.

Is there a fix or remedy for this issue?

The recall record does not specify a remedy.

Take action

Contact Brewer

We’ve drafted a message you can send Brewer to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2531-2018 — Brewer Brewer

Hello,

I own a Brewer that is covered by recall Z-2531-2018 from Brewer.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2531-2018 (March 29, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2531-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 21, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Brewer Company, LLC recalls Access Hi-Low Exam Tables, Model 6501-XX

Lower-risk recall