Gf Health Products recalls Drop Arm Versamode model 6810A due to incorrect casters. Affected units sold with specific lot numbers and identifiers.
The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
Gf Health Products is recalling the Drop Arm Versamode model 6810A because its front casters are incorrect. This could cause instability or accidents if the device is used without proper caster alignment.
The front casters being incorrect means the device may not move smoothly or stay stable when in use. This could lead to instability or accidents if the device is not properly aligned.
Users of the Drop Arm Versamode model 6810A with the specific lot number BMW316BS or device identifier M36868101 are affected. Those who use the device for medical purposes are most at risk.
Check for the model number 6810A on the device. Affected units have the lot number BMW316BS or device identifier M36868101.
Look for the model number 6810A, lot number BMW316BS, or device identifier M36868101 on the product.
The model number is 6810A.
The affected lot number is BMW316BS.
The device identifier is M36868101.
We’ve drafted a message you can send Gf Health Products to request your refund or repair — edit it as you like.
Subject: Recall Z-1353-2021 — Gf Health Products Gf Health Products Hello, I own a Gf Health Products that is covered by recall Z-1353-2021 from Gf Health Products. 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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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.
