# FDA recall Z-1139-2019

> **Pintler Medical LLC** · Class II · device recall initiated 2018-04-20.

## Product

A warming pad, a component of the PINTLER PEAK & PINTLER SUMMIT Heated OR pad.  PPWS-001     indicated for use in any condition where patient warming is desired as determined by clinical personnel, in accordance with facility normo-thermia protocol

## Reason for recall

Malfunction warming pad.

## Distribution

US Distribution to state of: Wisconsin.

## Key facts

- **Recall number:** Z-1139-2019
- **Recalling firm:** Pintler Medical LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2018-04-20
- **Report date:** 2019-04-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Philipsburg, MT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1139-2019

## Citation

> AI Analytics. FDA recall Z-1139-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1139-2019. Source: US FDA. Licensed CC0.

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