Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT recall — FDA Z-1500-2026
The device does not bear a unique device identifier.
Overview of recall records associated with Penner Patient Care, Inc., including dates, categories and classifications where available.
Classification mix: Class III: 1.
The device does not bear a unique device identifier.
This page summarizes recall records in which the official source identifies Penner Patient Care, 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.