PROVIDENCE MEDICAL TECHNOLOGIES: Medical Device Recall in 2020 - (Recall #: Z-2428-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation appropriate for the size of the device. Screws are intended for single use only. L Providence Medical Technology, Inc. 3875 Hopyard Road, Suite 300, Pleasanton, CA 94588, Rx Only.

Product Classification:

Class II

Date Initiated: March 29, 2019

Date Posted: July 1, 2020

Recall Number: Z-2428-2020

Event ID: 85111

Reason for Recall:

There may be dimensional manufacturing error that represents a potential safety risk to patients.

Status: Terminated

Product Quantity: 208 units

Code Information:

Model Number; PD 32 601 - ALLY Bone Screw L 10mm Lot Number: 046164 Model Number: PD 32 602 - ALLY Bone Screw L 12mm Lot Numbers: 045375 045646 045647 046313

Distribution Pattern:

US Nationwide distribution including in the states of AZ, CA, FL, IL, IN, LA, MA, MO, NC, NJ, NY, OH, OR and TX.

Voluntary or Mandated:

Voluntary: Firm initiated