# FDA recall Z-2033-2018

> **Joerns Healthcare** · Class II · device recall initiated 2018-05-03.

## Product

P.R.O. Matt:  (a) PROMATT PLUS 36 X 76 MATRESS, NYLON,  MATERIAL NUMBER PMP3676NZBA  (b) PROMATT PLUS 84" MATRESS, NYLON,  MATERIAL NUMBER PMP3684NZBA  (c) PROMATT PLUS W/SIDEWALLS, 42X80,  MATERIAL NUMBER PMS4280NZBA  (d) PROMATT PLUS 36IN MATRESS, MATERIAL NUMBER PMP3680NZBA  (e) PROMATT WITH SIDEWALLS ASSEMBLY,  MATERIAL NUMBER PMS3680NZBA  (f) PROMATT PLUS 80IN MATRESS, STRETCH,  MATERIAL NUMBER PMP3680SZBA  (g) PROMATT PLUS 42IN MATRESS, MATERIAL NUMBER PMP4280NZBA  (h) PROMATT PLUS 85cm MATRESS, DURATUB,  MATERIAL NUMBER PMPE3480SZBADT    Product Usage:  Non powered flotation therapy mattress. The device is intended to treat or prevent decubitus ulcers (bed sores).

## Reason for recall

Joerns Healthcare has identified a potential issue with some of the P.R.O. Matt and ProCair Mattresses.  For the identified serial number range of P.R.O. Matt and ProCair Mattresses incorrect connectors (part #s 206-0401 & 206-0405) were provided by a Joerns supplier without the required internal shutoff valves, these shutoff valves prevent air from escaping from the mattress air cells.

## Distribution

Worldwide Distribution - US Nationwide in the states of UK, Canada, Holland

## Key facts

- **Recall number:** Z-2033-2018
- **Recalling firm:** Joerns Healthcare
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-03
- **Report date:** 2018-06-06
- **Termination date:** 2023-09-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arlington, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2033-2018

## Citation

> AI Analytics. FDA recall Z-2033-2018. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2033-2018. Source: US FDA. Licensed CC0.

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