Z-1429-2020 Class II Ongoing
FDA device recall Z-1429-2020 was initiated by Seca on Jun 19, 2019 and is designated Class II. 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… The recall status is ongoing. Affected quantity: 254 scale carts.
Recall details
- Product Type
- Devices
- Report Date
- Mar 11, 2020
- Initiation Date
- Jun 19, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 254 scale carts
Product description
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 pattern
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
Code information
serial numbers: 6002142000002 - 6002142001101
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1429-2020
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026