Penner Patient Care, Inc.: Bath, Hydro-massage
Penner Patient Care is recalling certain Penner Pacific Bathing Spa models (350010-1, 350000-2, and 350010-X) distributed nationwide because they lack a required unique device identifier. This is a Class II recall, meaning the product could cause serious health consequences but is not expected to cause death. The affected spas were sold across all U.S. states and the District of Columbia.
- Recalling firm
- Penner Patient Care, Inc.
- Product
- Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X
- Reason
- The device does not bear a unique device identifier.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2025-08-13
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/49f09c4a-a6f5-4a80-941c-04e5b78b1016