Recall Z-2217-2017— Cardinal Scale Mfg Co
Class II · Terminated
Class II FDA medical device recall by Cardinal Scale Mfg Co, initiated 2015-12-23, terminated 2017-06-28. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Cardinal Scale Mfg Co
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-12-23
- Terminated
- 2017-06-28
- Firm location
- Webb City, MO, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.