JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 3-4 , REF 74013987 The JOURNEY II XR Tibial Posterior Keel Punch is a reusable surgical instrument used to prepare the proximal tibial to receive a JOURNEY II XR tibial baseplate.
Reported: April 3, 2019 Initiated: December 10, 2018 #Z-1043-2019
Product Description
JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 3-4 , REF 74013987 The JOURNEY II XR Tibial Posterior Keel Punch is a reusable surgical instrument used to prepare the proximal tibial to receive a JOURNEY II XR tibial baseplate.
Reason for Recall
Higher than anticipated occurrence of bone fracture during the use of the XR Tibia Posterior Punch
Details
- Recalling Firm
- Smith & Nephew, Inc.
- Units Affected
- 65 units
- Distribution
- US Distribution to OR and TN; and Internationally to: Japan.
- Location
- Memphis, TN
Frequently Asked Questions
What product was recalled? ▼
JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 3-4 , REF 74013987 The JOURNEY II XR Tibial Posterior Keel Punch is a reusable surgical instrument used to prepare the proximal tibial to receive a JOURNEY II XR tibial baseplate.. Recalled by Smith & Nephew, Inc.. Units affected: 65 units.
Why was this product recalled? ▼
Higher than anticipated occurrence of bone fracture during the use of the XR Tibia Posterior Punch
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 3, 2019. Severity: Moderate. Recall number: Z-1043-2019.
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