ADAPTABLE Beach Chair Beach Chair Surgical Patient Positioner
The Adaptable Beach Chair surgical patient positioner has a manufacturing issue with an inadequate weld for the head positioning system.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
QUANTUM OPS Inc began a recall of the ADAPTABLE Beach Chair surgical patient positioner on July 24, 2026, due to a manufacturing issue involving an inadequate weld for the patient head positioning system. The FDA added the recall to its Enforcement Report and classified it on October 2, 2026.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the list below, then check the codes the FDA notice also names.
- Model
- 804-33-300
- 3105-400-030
- Lot
- 2021110101
- 2021120201
- 2022010601
- 2023012501
- 2023020201
- 2023060101
- 2023071801
- 2024081401
- 2024091001
- 2024100301
- 2024110401
- 2020102701
- 2021050601
- 2022031701
- 2023020101
- 2023032001
From the FDA notice
Model/Catalog Number: 804-33-300 (Enovis); 3105-400-030 (Stryker); internal BC-0001 / BC-0220
Details
- Company began the recall
- Event ID
- 99384
- Company
- QUANTUM OPS Inc
- Hazard
- Manufacturing deviation
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
