PlainRecalls
FDA Devices Moderate Class II Terminated

Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW, QTY: (1), STERILE R, REF 71801306 Orthopedic

Reported: April 26, 2017 Initiated: March 9, 2017 #Z-1854-2017

Product Description

Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW, QTY: (1), STERILE R, REF 71801306 Orthopedic

Reason for Recall

The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.

Details

Recalling Firm
Smith & Nephew, Inc.
Units Affected
1 unit
Distribution
Worldwide Distribution - US (Nationwide) Internationally to Colombia, Denmark, Finland, France, Great Britain, Italy, and Singapore
Location
Memphis, TN

Frequently Asked Questions

What product was recalled?
Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW, QTY: (1), STERILE R, REF 71801306 Orthopedic. Recalled by Smith & Nephew, Inc.. Units affected: 1 unit.
Why was this product recalled?
The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 26, 2017. Severity: Moderate. Recall number: Z-1854-2017.