Aurora, NE, United States
Penner Patient Care, Inc. recalls
1 recall recorded since 2018, most recently on 13 August 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class III Medical devices
- Recall started
- 13 August 2025
- Reason
- The device does not bear a unique device identifier.
- Distribution
- US Nationwide distribution.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1502-2026, Z-1501-2026, Z-1503-2026, Z-1507-2026, Z-1500-2026, Z-1504-2026, Z-1508-2026, Z-1506-2026, Z-1499-2026, Z-1505-2026
- Penner Pacific Bathing Spa, Model Numbers 360020-1P
- Penner Pacific Bathing Spa, Model Numbers 360020-1EP
- Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 360030-1CTS, 360030-XCTS, 3600301-CTS, 360030-XCE, 360030-1CT, 360030-1CE
- Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1
- Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 370000-XWL, 360010-1WTL, 360010-XWT, 360010-2, 370000-2W, 360010-2L, 370000-
- Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X
- Penner Pacific Bathing Spa, Model Numbers 860010-1L
- Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
- and 2 more product lines
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.