Facility

Penner Patient Care, INC

1 recall(s) on record — most severe on record: Class III.

Key facts

1recalls · worst Class III

2inspections · worst VAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	1922538
Establishment type	Manufacture Medical Device
Location	101 Grant St Aurora, NE, US 68818
Registration status	Active · expires 2026
Parent company	Penner Patient Care, INC (owner-operator 9041224)
Brand names	PACIFIC

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (1)

Bath, Hydro-Massage
Product code ILJ (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.5100

Recalls & enforcement

Class IIIOngoing2025-08-13
The device does not bear a unique device identifier.

FDA inspections (2)

VAI2025-02-11
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
VAI2016-06-21
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by Penner Patient Care, INC

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Penner Patient Care, INC (FEI 1922538) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1922538-penner-patient-care-inc/

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