ADAPTABLE Beach Chair Beach Chair surgical patient positioner recall — FDA Z-0076-2027
Due to a manufacturing issue (inadequate weld) for patient head positioning system.
Overview of recall records associated with QUANTUM OPS Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Due to a manufacturing issue (inadequate weld) for patient head positioning system.
This page summarizes recall records in which the official source identifies QUANTUM OPS Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.