PlainRecalls

Devicor Medical Products Inc

Compiled from official public sources by the publisher.

5 recalls on record · Latest: Jun 3, 2026

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Agency notice ledger

Federal filing book Devicor Medical Products Inc LIGHT-BOOK · SINGLE-AGENCY

#2,441 of 14,151 · 5 notices · 0.005% archive

  • BOOK 5 notices
  • RANK #2,441 of 14,151
  • SHARE 0.005% archive
  • AGENCY FDA Devices (5)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 3, 2026
  • PHOTO A G Specialty Foods I…

Nearest notice-volume peer: A G Specialty Foods Inc (0 notice gap)

Devicor Medical Products Inc accounts for about 0.005% of the 104,423-notice archive on 5 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 →

Devicor Medical Products Inc's standing among 14,151 recalling firms

Devicor Medical Products Inc ranks 2,441st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Devicor Medical Products Inc vs all firms by recall-notice count

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

5 2441st of 14151 higher than 11,411 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 · 2026-09-13

Devicor Medical Products Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Devicor Medical Products Inc holds about 0.005% of archive notices alongside 5 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jun 3, 2026

HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3
FDA Devices Moderate Jun 1, 2022

HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4
FDA Devices Low Oct 14, 2020

Neoprobe GDS Control Unit, Model Number NPCU3
FDA Devices Moderate Mar 29, 2017

Mammotome Revolve Dual Vacuum Assist Biopsy System The device is used to sample breast tissue that has been identified as suspicious under imaging guidance
FDA Devices Moderate Jul 20, 2016

Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009 & MST0815. Each disposable probe is packaged within a thermoformed tray and covered with a pre-printed (product code and graphics) Tyvek lid. Each tray is labeled on-demand after sealing with a lot number and expiration date. Trays are kitted into sets of five probes and packaged within a sales carton. Two sales cartons are then packed into a corrugated case and shipped to the global distribution center. Device is labeled

Devicor Medical Products Inc 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 Devicor Medical Products Inc? ▼
PlainRecalls indexes 5 distinct federal recall events naming Devicor Medical Products Inc, 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 Devicor Medical Products Inc sit among other recalling firms? ▼
Devicor Medical Products Inc ranks #2,441 of 14,151 by distinct recall-event count among 14,151 firms in this archive (81st percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Devicor Medical Products Inc's notices? ▼
FDA Devices accounts for 5 of this firm's 5 indexed notices.
What product category dominates Devicor Medical Products Inc's filing book? ▼
Filings for Devicor Medical Products Inc 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.
Devicor Medical Products Inc: 5 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 Devicor Medical Products Inc; individual notices remain authoritative on each linked recall page.

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