Stop using now Medical device recall · FDA · Published July 24, 2026

ADAPTABLE Beach Chair Surgical Patient Positioner Recall: Inadequate Weld Risk

ADAPTABLE Beach Chair surgical patient positioners with inadequate welds in the head positioning system are recalled. These devices risk patient injury during surgery. Stop using immediately and contact the manufacturer for a replacement.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0076-2027Medical device ADAPTABLE ›

Stop using this now

Due to a manufacturing issue (inadequate weld) for patient head positioning system.

✎ GovInfoNow plain-language explainer

ADAPTABLE recalls surgical beach chairs that can cause patient injury due to a weak weld in the head support area. This risk exists during surgery when the chair is used to elevate the patient's upper body. Read more at govinfonow.com/recall/1629784-quantum-ops-inc-recalls-brand-name-adaptable-beach-chair-product.

Source Summary by GovInfoNow · govinfonow.com/recall/1629784-quantum-ops-inc-recalls-brand-name-adaptable-beach-chair-product · Updated October 21, 2026 · FDA enforcement record: FDA #Z-0076-2027

Cite this page

“ADAPTABLE Beach Chair Surgical Patient Positioner Recall: Inadequate Weld Risk.” GovInfoNow, updated October 21, 2026. https://govinfonow.com/recall/1629784-quantum-ops-inc-recalls-brand-name-adaptable-beach-chair-product. Based on FDA recall #Z-0076-2027 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0076-2027%22&limit=1).

The FDA announced on July 24, 2026, that QUANTUM OPS Inc is recalling its ADAPTABLE Beach Chair surgical patient positioner due to an inadequate weld in the patient head positioning system. Owners should contact the company for a remedy.

How to tell if you have it

Brand: ADAPTABLE
Product Name: Beach Chair surgical patient positioner
Model/Catalog Number: 804-33-300 (Enovis)
Model/Catalog Number: 3105-400-030 (Stryker)
Internal codes: BC-0001 / BC-0220
GTIN / UDI-DI: 00190446667278
Product Number: 3105-400-030 Lots: 2021110101, 2021120201, 2022010601, 2023012501, 2023020201, 2023060101, 2023071801, 2024081401, 2024091001, 2024100301, 2024110401
Product Number: 804-33-300 Lot Numbers: 2020102701, 2021050601, 2022031701, 2023020101, 2023032001
Lot Number: 2020101201

The hazard

The recall is due to a manufacturing issue involving an inadequate weld in the patient head positioning system. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include SeaSpine Polyaxial Head Recall (2026-05-28) and Baxter Head Positioning Adapter May Become Loose on Operating Tables (2026-04-21). Additional recent recalls include Olympus HALO PKS Cutting Forceps Recall (2026-02-25).

How to tell if you have this one

Look for the product name 'Beach Chair surgical patient positioner' with model numbers 804-33-300 (Enovis) or 3105-400-030 (Stryker). Check serial numbers listed in the affected lots above.

Brand
ADAPTABLE
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using Immediately
Discard or remove the device from use immediately as it poses a risk of injury during surgery.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 2 states.

FDA distribution: “U.S. Nationwide distribution in the states of CA and TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: California, Texas.

Recall timeline

FDA published this recall 3 months after the firm started it.

Jul 24, 2026Firm started the recall
Oct 2, 2026FDA classified it Class II
Oct 14, 2026Published in FDA’s Enforcement Report
Oct 21, 2026Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

What serial numbers are affected?

Serial numbers from A-001 to A-024, C-032 to C-050, and others listed in the recall details.

Where was this product sold?

Sold nationwide in the U.S., specifically in California and Texas.

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Keep exploring

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Link to this recall

<a href="https://govinfonow.com/recall/1629784-quantum-ops-inc-recalls-brand-name-adaptable-beach-chair-product">ADAPTABLE Beach Chair Surgical Patient Positioner Recall: Inadequate Weld Risk (GovInfoNow)</a>

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-0076-2027 (July 24, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0076-2027 to see it in context.
Plain-language summary written by qwen3:4b on October 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.