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Moderate recall: A hazard has been identified, with no injuries reported yet. Follow the steps below.

Penner Patient Care, Inc. 2026-03-18 Health moderate FDA
Health · FDA · Recall #FDA-Z-1502-2026

Penner Pacific Bathing Spa, Model Numbers 360020-1P Recall

Issued March 18, 2026 · Penner Patient Care, Inc.

In March 2026, Penner Patient Care, Inc. recalled the Penner Pacific Bathing Spa, Model Numbers 360020-1P, a moderate health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

The device does not bear a unique device identifier.

What you should do

  1. 1 Stop using Penner Pacific Bathing Spa, Model Numbers 360020-1P right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Penner Patient Care, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Penner Patient Care, Inc.
Category
Health
Recall date
March 18, 2026
Units affected
Not reported
Sold at
US Nationwide distribution.
Recall number
FDA-Z-1502-2026
Made in
United States
Issuing agency
FDA

In context

  • Penner Patient Care, Inc. has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 356th Health recall we've logged in 2026.
Read the official FDA notice

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