FDA recall Z-1507-2026
Penner Patient Care, Inc. · Class III · device
Product
Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1
Reason for recall
The device does not bear a unique device identifier.
Distribution
US Nationwide distribution.
Key facts
- Status
- Ongoing
- Initiation date
- 2025-08-13
- Report date
- 2026-03-18
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Aurora, NE, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1507-2026