Riverpoint Medical, LLC: Medical Device Recall in 2023 - (Recall #: Z-0518-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Iconix Knotless 1.4mm Anchor with XBraid S (Black/White) REF 3911-714-521 The Iconix Knotless anchors are intended to be used for soft-tissue to bone fixation in the foot, ankle, knee, hip, hand, wrist, elbow and shoulder.

Product Classification:

Class II

Date Initiated: October 25, 2023

Date Posted: December 20, 2023

Recall Number: Z-0518-2024

Event ID: 93390

Reason for Recall:

Use of a 1.4 drill in hard bone conditions caused increased insertion forces leading to subsequent failures of the inserter, when the inserters bend, it may also move off the drill hole location leading to damage of the suture construct during insertion. Suture damage may lead to suture breaks during use.

Status: Ongoing

Product Quantity: 999 devices

Code Information:

Product Code: 3911-7 14-520 UDI-DI Code: 00840277402172 Lot Number: 23080433 Product Code: 3911-7 14-521 UDI-DI Code: 00840277402189 Lot Number: 23081617

Distribution Pattern:

U.S. Nationwide distribution in the state of CA.

Voluntary or Mandated:

Voluntary: Firm initiated