PlainRecalls
FDA Devices Moderate Class II Terminated

smith&nephew GENESIS(R) II TIBIAL Punch, 13 MM, REF 71440408, QTY: (1)

Reported: June 20, 2018 Initiated: May 4, 2018 #Z-2163-2018

Product Description

smith&nephew GENESIS(R) II TIBIAL Punch, 13 MM, REF 71440408, QTY: (1)

Reason for Recall

One lot of GENESIS II 13 mm tibial punches are 2 mm smaller than specification.

Details

Recalling Firm
Smith & Nephew, Inc.
Units Affected
5 units
Distribution
International only: United Arab Emirates, Spain, Mexico
Location
Memphis, TN

Frequently Asked Questions

What product was recalled?
smith&nephew GENESIS(R) II TIBIAL Punch, 13 MM, REF 71440408, QTY: (1). Recalled by Smith & Nephew, Inc.. Units affected: 5 units.
Why was this product recalled?
One lot of GENESIS II 13 mm tibial punches are 2 mm smaller than specification.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 20, 2018. Severity: Moderate. Recall number: Z-2163-2018.