Cardinal — Class II medical device recall Z-2217-2017
Terminated recall by Cardinal Scale Mfg Co, reported 2017-06-07, distributed nationwide. One complaint of a seat on a scale failing unexpectedly which can cause an injury.
| Recall number | Z-2217-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cardinal Scale Mfg Co, Webb City, MO, United States |
| Recall initiated | 2015-12-23 |
| Classified | 2017-06-01 |
| Reported by FDA | 2017-06-07 |
| Terminated | 2017-06-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, HK, KW, PK |
| Quantity | 975 scales |
| Model numbers | 1000, 600, 6868, 6876 |
Product
Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000
Reason for recall
One complaint of a seat on a scale failing unexpectedly which can cause an injury.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2217-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.