# FDA recall Z-3183-2018

> **Med-Mizer, Inc.** · Class II · device recall initiated 2018-07-25.

## Product

PR1000 Pivot Rehab Bed AC powered adjustable bed.

## Reason for recall

Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may become pinched.  A failure would result in the resident requiring to be transferred to a different bed until repairs can be made

## Distribution

The products were distributed to the following US states:  AR, AZ, FL, GA, IA, ID, IL, IN, KY, ME, MI, MN, MO, NC, ND, NE, NM, NY, OH, OK, PA, SC, SD, TN, TX, VA, WA, and WI.    The products were distributed to the following foreign countries:  Canada, China, and Denmark.

## Key facts

- **Recall number:** Z-3183-2018
- **Recalling firm:** Med-Mizer, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-25
- **Report date:** 2018-09-26
- **Termination date:** 2019-10-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Batesville, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3183-2018

## Citation

> AI Analytics. FDA recall Z-3183-2018. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-3183-2018. Source: US FDA. Licensed CC0.

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