PlainRecalls
FDA Devices Moderate Class II Ongoing

LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Tibial Insert

Reported: June 12, 2024 Initiated: March 29, 2024 #Z-1934-2024

Product Description

LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Tibial Insert

Reason for Recall

Due to unsupported 10 year expiration date.

Details

Recalling Firm
CORENTEC CO., LTD
Units Affected
397
Distribution
US Nationwide distribution in the states of AL, AZ, CA, MI, PA, TX.
Location
Cheonan, N/A

Frequently Asked Questions

What product was recalled?
LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Tibial Insert. Recalled by CORENTEC CO., LTD. Units affected: 397.
Why was this product recalled?
Due to unsupported 10 year expiration date.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 12, 2024. Severity: Moderate. Recall number: Z-1934-2024.