FDA Medical devices recall ·
Penner Pacific Bathing Spa, Model Numbers 360020-1P recall
- Recall number
- Z-1502-2026
- Date
- (initiated August 13, 2025)
- Company / brand
- Penner Patient Care, Inc.
101 Grant St, Aurora, NE, United States - Category
- Medical devices › Class III
- Classification
- Class III
- Status
- Ongoing
- Units affected
- 45 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Penner Pacific Bathing Spa, Model Numbers 360020-1P
Why was it recalled?
The device does not bear a unique device identifier.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI-DI: 0085007365403; Serial Numbers: 11193097601 10216195501 10216195502 12193104901 06226342101 06226342102 06226342105 06226342107 03203148701 01226259601 10226410801 06246724701 10203210401 10203210402 05216113101 11193095401 01203118301 05216107301 05216107302 05216107303 05216107304 05216107305 05216108301 05216108302 06193030201 03203147601 09193066601 03216060801 07193052301 09236591501 02246673801 02192976301 03246682701 01192960801 01192960802 06236535501 08152390701 03216065101 05182864901 01142094001 11121856201 03192998301 01192959801 01226256901 03256938801
Distribution
US Nationwide distribution.
What does Class III mean?
Class III means use of or exposure to the product is not likely to cause adverse health consequences (for example, a labeling violation).
Source: FDA (medical devices), recall Z-1502-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.