# FDA recall Z-2470-2021

> **Getinge Dominican Republic SA** · Class II · device recall initiated 2021-07-30.

## Product

Arjo Disposable Repositioning Sling, Model AHD001

## Reason for recall

Sling loop straps on device pose a trip hazard.

## Distribution

US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, MD, ME, MI, MN, MO, MS, NC, ND, NJ, NM, NY, OH, OR, PA, SC, TN, TX, VA, VT, WI, and WV.

## Key facts

- **Recall number:** Z-2470-2021
- **Recalling firm:** Getinge Dominican Republic SA
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-30
- **Report date:** 2021-09-22
- **Termination date:** 2023-08-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Itabo, Haina, N/A, Dominican Republic (the)

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2470-2021

## Citation

> AI Analytics. FDA recall Z-2470-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2470-2021. Source: US FDA. Licensed CC0.

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