PlainRecalls

Quantum Surgical Sas

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Jun 18, 2025

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Agency notice ledger

Federal filing book Quantum Surgical Sas LIGHT-BOOK · SINGLE-AGENCY

#5,605 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,605 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 18, 2025
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Quantum Surgical Sas accounts for about 0.002% of the 104,423-notice archive on 2 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Quantum Surgical Sas's standing among 14,151 recalling firms

Quantum Surgical Sas ranks 5,605th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Quantum Surgical Sas vs all firms by recall-notice count

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

2 5605th of 14151 higher than 8,037 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 · 2026-09-14

Quantum Surgical Sas in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Quantum Surgical Sas holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jun 18, 2025

EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is a user controlled, stereotactic accessory intended to assist in the planning and manual advancement of one or more instruments, as well as in verification of instrument position during Computed Tomography (CT) guided percutaneous ablation procedures in the abdomen, performed by physicians trained for CT procedures and performed under general anaesthesia with rigid straight instruments such as needles and probes of diamet
FDA Devices Moderate Oct 16, 2024

The EPIONE device v1.0.2 is a user controlled, stereotactic accessory device intended to assist in the planning and manual advancement of one or more instruments, as well as in verification of instrument position during Computed Tomography (CT) guided percutaneous procedures. During the planning phase, the desired instrument placement and performance is defined relative to the target anatomy. During the guidance phase, the device enables to monitor respiratory levels and verify patient position

Quantum Surgical Sas is a small archive contributor

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

Frequently Asked Questions

How many federal recall notices name Quantum Surgical Sas? ▼
PlainRecalls indexes 2 distinct federal recall events naming Quantum Surgical Sas, 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 Quantum Surgical Sas sit among other recalling firms? ▼
Quantum Surgical Sas ranks #5,605 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Quantum Surgical Sas's notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Quantum Surgical Sas's filing book? ▼
Filings for Quantum Surgical Sas 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.
Quantum Surgical Sas: 2 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 Quantum Surgical Sas; individual notices remain authoritative on each linked recall page.

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