Class II
Medical Device Recall: LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Tibial Insert
CORENTEC CO., LTD · March 29, 2024
Reason for Recall
Due to unsupported 10 year expiration date.
Distribution
US Nationwide distribution in the states of AL, AZ, CA, MI, PA, TX.
States Affected
NATIONWIDE
Quantity Affected
397
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1934-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.