Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1504-2026 — 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

U.S. FDA — Device Enforcement · United States · 2025-08-13 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1504-2026
Date of alert: 2025-08-13
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Penner Patient Care, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 0085007365405

Reported risk: The device does not bear a unique device identifier.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-1504-2026 — 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

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