PlainRecalls

Zavation

71 recalls on record · Latest: Jun 9, 2021

Subscribe to new Zavation recalls (RSS)

Agency notice ledger

Federal filing book Zavation MID-BOOK · SINGLE-AGENCY

#254 of 14,151 · 71 notices · 0.068% archive

  • BOOK 71 notices
  • RANK #254 of 14,151
  • SHARE 0.068% archive
  • AGENCY FDA Devices (71)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 9, 2021
  • PHOTO Acura,Honda

Nearest notice-volume peer: Acura,Honda (0 notice gap)

Zavation accounts for about 0.068% of the 104,423-notice archive on 71 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Zavation's standing among 14,151 recalling firms

Zavation ranks 254th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Zavation vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

71 254th of 14151 higher than 13,897 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-10-30

Zavation in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Zavation holds about 0.068% of archive notices alongside 71 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of October 2026
FDA Devices Moderate Jun 9, 2021

10G DIRECT SINGLE BONE ACCESS KIT. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

ZVplasty 10G, 20mm, Traditional Unipedicular Kit, REF VCF-1020-1. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

ZVplasty Direct Unipedicular Bone Access Kit with Drill, 10 Gauge, REF VCF-DSBAK. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

ZVplasty Direct Access Bevel Tip Trocar, 11 Gauge, REF VCF-1022-11. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

10 GAUGE DIRECT UNILATERAL STYLET (1 X DIAMOND 1 X BEVEL) STERILE. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

ZVplasty Direct Access Diamond Tip Trocar, 10 Gauge, REF VCF-1023. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

10 GAUGE DIRECT ACCESS DIAMOND TIP, CODE: INTVM-DWCd. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

ZVplasty System, 20mm, Part# VCF-1020-2. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

InterV, 10G Kyphoplasty Kits, REF numbers: a) INTVM-10-DSK b) INTVM-10-SBK c) INTVM-15-DSK d) INTVM-15-DSKC e) INTVM-15-SBK f) INTVM-15-SIKBC g) INTVM-20-DSK h) INTVM-20-SBK. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

OsteoFlex Cement and Mixing System, REF VCF-OSFL. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

10G COAXIAL CANNULA WITH TUOHY CONNECTION STERILE. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

11G DIRECT DOUBLE BONE ACCESS KIT. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

InterV 10G Bone Access Tools/Kit, REF INTVM-FLNK. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

ZVplasty Direct Bipedicular Bone Access Kit with Drill, 11 Gauge, REF VCF-DDBAK-11. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

10 G Coxaxial Cannula with Tuohy Connection, CODE: INTVM-CC. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL), CODE INTVM-DSSKbd. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

10G BEVELED TROCAR/CANNULA. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

CEMIX - CEMENT MIXING SYSTEM STERILE, CODE INTV-MMS. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

ZVplasty Cement Delivery Cannula, REF VCF-1007. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

ZVplasty, Direct Bipedicular, Bone Access Kit with Coxaial Cannula, REF VCF-DDSKbd. For use in Orthopedic / spinal procedures.

FDA Devices Moderate Jun 9, 2021

ZVplasty Biopsy Device, 11 Gauge, REF VCF-1010-11. For use in Orthopedic / spinal procedures.

Zavation carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (71 here — heavy-book).

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Frequently Asked Questions

How many federal recall notices name Zavation? ▼
PlainRecalls indexes 71 distinct federal recall events naming Zavation, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of October 2026). That count is an issuance inventory, not a hazard score.
Where does Zavation sit among other recalling firms? ▼
Zavation ranks #254 of 14,151 by distinct recall-event count among 14,151 firms in this archive (98th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Zavation's notices? ▼
FDA Devices accounts for 71 of this firm's 71 indexed notices.
What product category dominates Zavation's filing book? ▼
Filings for Zavation span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Zavation: 71 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Zavation; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of October 2026