Flower Orthopedics Corporation: Medical Device Recall in 2021 - (Recall #: Z-0034-2022)

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:

Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201

Product Classification:

Class II

Date Initiated: September 3, 2021

Date Posted: October 13, 2021

Recall Number: Z-0034-2022

Event ID: 88724

Reason for Recall:

Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws) from EWK 201 (Flower E-Kit, Advanced)

Status: Terminated

Product Quantity: 77 kits

Code Information:

Lot Number: 2104321637 Unique Identifier: 00840118112079

Distribution Pattern:

US Nationwide distribution in the states of AZ, CA, CO,CT, FL, IL, IN, NC, NY, NV, OH, WV, TX.

Voluntary or Mandated:

Voluntary: Firm initiated