FDA Device recall Z-2217-2017
Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000
- FDA Device
- Class II
- terminated
- Published 2017-06-07
On 2017-06-07 the FDA classified a Class II recall of Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000 by Cardinal Scale Mfg, citing one complaint of a seat on a scale failing unexpectedly which can cause an injury.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2217-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-12-23 |
| Published | 2017-06-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Cardinal Scale Mfg |
| Distribution | US |
Product
Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000
Reason
One complaint of a seat on a scale failing unexpectedly which can cause an injury.
Identifiers
| code_info | None. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2217-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.