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 from Penner Patient Care, Inc. 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.
Firm name as filed with the FDA: “Penner Patient Care, Inc.”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.