Drop Arm Versamode (Gf Health) – Caster Problem (2021)
Incorrect medical device casters can potentially create operational and safety challenges.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Drop Arm Versamode"
Brand
Gf Health Products
Lot Codes / Batch Numbers
Model: 6810A, Device Identifier: M36868101, and Lot number: BMW316BS
Products Sold
Model: 6810A; Device Identifier: M36868101; and Lot number: BMW316BS
Gf Health Products is recalling Drop Arm Versamode" due to The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
Recommended Action
Per FDA guidance
A Recall notification letter titled, "URGENT CORRECTION AND REMOVAL" was sent to consignees on 03/24/2021 via FedEx priority. The consignees were instructed to: "The replacement of the front casters is required to ensure proper operation of the Versamode, and to eliminate any potential safety concern. 1. Contact GF Health Products at 1-888-974-4347 or fieldcorrection@grahamfield.com within ten (10) business days from receipt of this notification to schedule your front caster replacement order. Replacement front casters will be provided at NO CHARGE for Versamodes with lot number BMW316BS. 2. Upon receipt of the replacement casters, follow the enclosed instructions Replacing Your Lumex Drop Arm Versamode Front Casters. (Attachment 1) 3. Dispose of the incorrect, replaced casters in accordance with Federal, State, or Local regulations. 4. Fill out and sign the Certification of Replacement Agreement. (Attachment 2) 5. Return the completed Certification of Replacement Agreement to: fieldcorrection@grahamfield.com or Fax: 770-368-3333."
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026