Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Flower E-Kit Recalled by Flower Orthopedics Corporation Due to Product kit missing CDG 200 (Cannulated Countersink for...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Flower Orthopedics Corporation directly.
Affected Products
Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
Quantity: 77 kits
Why Was This Recalled?
Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws) from EWK 201 (Flower E-Kit, Advanced)
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Flower Orthopedics Corporation
Flower Orthopedics Corporation has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report