PlainRecalls

Zavation

Compiled from official public sources by the publisher.

71 recalls on record · Latest: Jun 9, 2021

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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 · 2026-09-15

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 September 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).

Acura,Honda 71 American Pharmaceutical Ingredients LLC 71 Bj Wholesale Club 71 Giant Eagle 71 Inventure Foods 71

Similar medical devices volume

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

Karl Storz Endoscopy 71 Heartware, Inc. 72 Alcon Research LLC 70 Ethicon, Inc. 70

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 September 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 September 2026