Flower Orthopedics Corporation: Medical Device Recall in 2021 - (Recall #: Z-1698-2021)

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:

T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits (GWK 300) - Product Usage: Intended to be used to insert screws with T25 driving features, which includes screws with diameters of 5.5mm, 6.5mm, and 7.3mm Product Code: GWK 300

Product Classification:

Class II

Date Initiated: April 15, 2021

Date Posted: June 9, 2021

Recall Number: Z-1698-2021

Event ID: 87906

Reason for Recall:

Cannulated Screwdrivers may break at the driver tip along the shaft, near the handle extending surgery time and additional x-ray to identify the fragments from the breakages

Status: Terminated

Product Quantity: 47 units

Code Information:

Lot Numbers: 2003320898, 1810220041, 1802220008, 1802220005, 1711220035 UDI: 00840118110853

Distribution Pattern:

US Nationwide distribution in the states of AZ, CO, FL, GA, IL, IN, PA, NC, VA.

Voluntary or Mandated:

Voluntary: Firm initiated