Orthofix, Inc: Medical Device Recall in 2018 - (Recall #: Z-2130-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

L-Plate, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Left or Right (Part Number): a) Left (003-E-00001L); b) Right (003-E-00001R)

Product Classification:

Class II

Date Initiated: April 6, 2018

Date Posted: June 13, 2018

Recall Number: Z-2130-2018

Event ID: 79819

Reason for Recall:

Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating System and Rival View Plating System. As the result of a complaint investigation, the locking screws were confirmed to not properly engage the plates during surgery.

Status: Terminated

Product Quantity: 30

Code Information:

(UDI)/Lot: a) (18056099647830) B1108952; b) (18056099647847) B1108955

Distribution Pattern:

U.S Consignees: NJ, FL, PA, SC, LA, VA, MN, TX, GA, DC, NV, IN, CA, MI, IL, MD, NC, OH, OK,

Voluntary or Mandated:

Voluntary: Firm initiated