Smith & Nephew, Inc.: Medical Device Recall in 2021 - (Recall #: Z-1510-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Usage: used for interference fixation of bone-tendon-bone of soft tissue grafts in anterior cruciate ligament reconstruction, Part Number: 014208

Product Classification:

Class II

Date Initiated: April 8, 2021

Date Posted: May 5, 2021

Recall Number: Z-1510-2021

Event ID: 87717

Reason for Recall:

Mislabeled box contained a 6mm x 20mm screw instead of 6mm x 30mm screw

Status: Terminated

Product Quantity: 2 units US and 193 units OUS. 195 units WW

Code Information:

Lot Number: 50906647

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the state of FL and the countries of Australia, Japan.

Voluntary or Mandated:

Voluntary: Firm initiated