Theken Companies LLC: Device Recall

Recall #Z-0227-2026 · 09/11/2025

Class II: Risk

Recall Details

Recall Number: Z-0227-2026
Classification: Class II
Product Type: Device
Recalling Firm: Theken Companies LLC
Status: Ongoing
Date Initiated: 09/11/2025
Location: Akron, OH, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 409

Reason for Recall

Downstream recall for RES 97605, BioPro femoral components. Product failed transit testing. Impacted product may have potential issues with sterile barrier.

Product Description

iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Assembly, Size 38mm 10-22-0040 Bipolar Head Assembly, Size 40mm 10-22-0042 Bipolar Head Assembly, Size 42mm 10-22-0044 Bipolar Head Assembly, Size 44mm 10-22-0046 Bipolar Head Assembly, Size 46mm 10-22-0048 Bipolar Head Assembly, Size 48mm 10-22-0050 Bipolar Head Assembly, Size 50mm 10-22-0052 Bipolar Head Assembly, Size 52mm 10-22-0054 Bipolar Head Assembly, Size 54mm 10-22-0056 Bipolar Head Assembly, Size 56mm 10-22-0058 Bipolar Head Assembly, Size 58mm 10-22-0060 Bipolar Head Assembly, Size 60mm

Distribution Pattern

US Nationwide distribution in the states of NJ, PA, and TX.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.