PlainRecalls

Pro-Med Instruments Gmbh

Compiled from official public sources by the publisher.

5 recalls on record · Latest: Jun 4, 2025

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Agency notice ledger

Federal filing book Pro-Med Instruments Gmbh LIGHT-BOOK · SINGLE-AGENCY

#2,619 of 14,151 · 5 notices · 0.005% archive

  • BOOK 5 notices
  • RANK #2,619 of 14,151
  • SHARE 0.005% archive
  • AGENCY FDA Devices (5)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 4, 2025
  • PHOTO A G Specialty Foods I…

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

Pro-Med Instruments Gmbh 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 →

Pro-Med Instruments Gmbh's standing among 14,151 recalling firms

Pro-Med Instruments Gmbh ranks 2,619th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Pro-Med Instruments Gmbh vs all firms by recall-notice count

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

5 2619th 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

Pro-Med Instruments Gmbh in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Pro-Med Instruments Gmbh 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 4, 2025

DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)
FDA Devices Critical Sep 26, 2018

DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries
FDA Devices Critical Sep 26, 2018

DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries
FDA Devices Critical Sep 26, 2018

DORO LUCENT Locking Transitional Member, REF 1101.031 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries
FDA Devices Moderate Dec 13, 2017

pmi, pro med instruments, DORO(R) Sterile Disposable Skull Pins, 3 pieces (3 pieces per blister, 12 blisters per box), STERILE R, Rx ONLY The DORO(R) Skull Pins are inserted into the receptacles of the skull clamp and fixate the head during surgery.

Pro-Med Instruments Gmbh 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 Pro-Med Instruments Gmbh? ▼
PlainRecalls indexes 5 distinct federal recall events naming Pro-Med Instruments Gmbh, 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 Pro-Med Instruments Gmbh sit among other recalling firms? ▼
Pro-Med Instruments Gmbh ranks #2,619 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 Pro-Med Instruments Gmbh's notices? ▼
FDA Devices accounts for 5 of this firm's 5 indexed notices.
What product category dominates Pro-Med Instruments Gmbh's filing book? ▼
Filings for Pro-Med Instruments Gmbh 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.
Pro-Med Instruments Gmbh: 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 Pro-Med Instruments Gmbh; individual notices remain authoritative on each linked recall page.

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