iTotal Identity Posterior Stabilised (PS) Knee Replacement System Model Number: TPS-301-1113-020101
Reported: April 20, 2022 Initiated: February 22, 2022 #Z-0899-2022
Product Description
iTotal Identity Posterior Stabilised (PS) Knee Replacement System Model Number: TPS-301-1113-020101
Reason for Recall
Incorrect tibial base plate implant packaged in kit
Details
- Recalling Firm
- Conformis, Inc.
- Units Affected
- 1 unit
- Distribution
- MS
- Location
- Billerica, MA
Frequently Asked Questions
What product was recalled? ▼
iTotal Identity Posterior Stabilised (PS) Knee Replacement System Model Number: TPS-301-1113-020101. Recalled by Conformis, Inc.. Units affected: 1 unit.
Why was this product recalled? ▼
Incorrect tibial base plate implant packaged in kit
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 20, 2022. Severity: Moderate. Recall number: Z-0899-2022.
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