“Gf Health Products Drop Arm Versamode 6810A: Incorrect Casters Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62988-gf-health-products-drop-arm-versamode-6810a-incorrect-casters-hazard. Based on FDA recall #Z-1353-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1353-2021%22&limit=1).
Gf Health Products voluntarily recalled the Drop Arm Versamode model 6810A due to incorrect front casters, according to the FDA on March 24, 2021.
How to tell if you have it
Brand: Gf Health Products
Product: Drop Arm Versamode
Model: 6810A
Device Identifier: M36868101
Lot number: BMW316BS
The hazard
The front casters on the recalled units are incorrect. The FDA classified this as a Class II recall involving 66 units distributed nationwide to CA, WI, PA, IL, and TX, as well as internationally to Mexico and Canada.
How to tell if you have this one
Check for the model number 6810A on the device. Affected units have the lot number BMW316BS or device identifier M36868101.
Brand
Gf Health Products
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Device Details
Look for the model number 6810A, lot number BMW316BS, or device identifier M36868101 on the product.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 5 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Distributed nationwide to CA, WI, PA, IL, and TX. Distributed internationally to Mexico and Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Illinois, Pennsylvania, Texas, Wisconsin.
Recall timeline
FDA terminated this recall 2.1 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-1353-2021 (March 24, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1353-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.