# FDA recall Z-1429-2020

> **Seca** · Class II · device recall initiated 2019-06-19.

## Product

Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009

## Reason for recall

It has been determined that the wheels on the baby scale cart can unexpectedly loosen and in the worst case, detach from the cart completely. If this occurs the cart can become unstable and tip over, potentially leading to the scale falling from the cart.  If a baby is left unattended in a cart, the baby could fall off the scale and be subjected to several serious injuries.

## Distribution

US: CA, MI, WA, WV, VA, NM, LA, TN, IL, PA, OH, FL, WA, OR, NY, CO, IA, MN, TX, MA, NC, LA, KY, NM AL,DC, NJ, AK, AZ, NV, SC, HI, MD, WI, RI, DE, MO    OUS: Canada

## Key facts

- **Recall number:** Z-1429-2020
- **Recalling firm:** Seca
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-06-19
- **Report date:** 2020-03-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hamburg, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1429-2020

## Citation

> AI Analytics. FDA recall Z-1429-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1429-2020. Source: US FDA. Licensed CC0.

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