Zavation recalls

Zavation has 71 recalls on record with the FDA and USDA, the earliest in 2021 and the latest reported on 9 Jun 2021. The most frequent reason is sterility.

Total recalls71since 2021

Last 12 months0reported

Class I00% of total

Ongoing0latest 9 Jun 2021

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 71 100%Class III 0 0%

Why zavation is recalled

Sterility71100%

Product types

Hip & Knee Implants4969%
Heart & Vascular Devices2231%

By year

202171100%

All zavation recalls, newest first

71 total

Reported	Class	Recall	Company	Reason	Where
9 Jun 2021Device	CLASS II	ZVplasty Biopsy Device recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty, Direct Bipedicular, Bone Access Kit with Coxaial Cannula recalled	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty Cement Delivery Cannula recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Cemix - Cement Mixing System Sterile recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Beveled Trocar/cannula recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Direct Unilateral Stylet(1 X Diamond 1 X Bevel) recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Coxaxial Cannula with Tuohy Connection recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty Direct Bipedicular Bone Access Kit with Drill recalled	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	InterV Bone Access Tools/Kit recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Direct Double Bone Access Kit recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Coaxial Cannula With Tuohy Connection Sterile recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	OsteoFlex Cement and Mixing System recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	InterV Kyphoplasty Kits recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty System, Part# VCF recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Direct Access Diamond Tip recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty Direct Access Diamond Tip Trocar recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Direct Unilateral Stylet (1 X Diamond 1 X Bevel) Sterile recalled	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty Direct Access Bevel Tip Trocar recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty Direct Unipedicular Bone Access Kit with Drill recalled	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty, Traditional Unipedicular Kit recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Direct Single Bone Access Kit recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty Single Balloon Kit recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	OsteoFlex Bone Cement recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Vertebrex Single Balloon Kit recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVPlasty Traditional Bipedicular Kit recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty Direct Access Diamond Tip Trocar recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Direct Unilateral Stylet(1 X Diamond 1 X Bevel), Intvm-dsskbd recalled	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty, Additional Level Kit recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	ZVplasty, Bipedicular Cement Delivery Cannula Kit recalled by Zavation	Zavation	Sterility	Nationwide
9 Jun 2021Device	CLASS II	Direct Single Bone Access Kit recalled by Zavation	Zavation	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.