Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa
The device does not bear a unique device identifier.
- Hydro-Massage Bath
- Error in labeling
The FDA has posted 10 enforcement recalls of hydro-massage bath devices since 2025, none of them Class I (most serious). Most recent report: Mar 18, 2026.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
Source: U.S. FDA openFDA device enforcement reports, updated continuously. Device type per the FDA's RES classification (“Bath, Hydro-Massage”). Informational only — verify against the FDA before acting.