PlainRecalls

Leonhard Lang Medizintechnik GmbH

Compiled from official public sources by the publisher.

4 recalls on record · Latest: Sep 20, 2017

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Agency notice ledger

Federal filing book Leonhard Lang Medizintechni… LIGHT-BOOK · SINGLE-AGENCY

#3,009 of 14,151 · 4 notices · 0.004% archive

  • BOOK 4 notices
  • RANK #3,009 of 14,151
  • SHARE 0.004% archive
  • AGENCY FDA Devices (4)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 20, 2017
  • PHOTO 1 Epic, LLC

Nearest notice-volume peer: 1 Epic, LLC (0 notice gap)

Leonhard Lang Medizintechnik GmbH accounts for about 0.004% of the 104,423-notice archive on 4 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 →

Leonhard Lang Medizintechni…'s standing among 14,151 recalling firms

Leonhard Lang Medizintechnik GmbH ranks 3,009th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Leonhard Lang Medizintechni… vs all firms by recall-notice count

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

4 3009th of 14151 higher than 10,859 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

Leonhard Lang Medizintechni… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Leonhard Lang Medizintechnik GmbH holds about 0.004% of archive notices alongside 4 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Critical Sep 20, 2017

Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion. Product Usage: Multifunction electrode for external defibrillation, pacing, cardioversion, and monitoring. The device is non-sterile and for single use only. Used with automated external defibrillators
FDA Devices Critical Oct 26, 2016

Skintact Electrodes for Defibrillation, DF29N. Product Usage: Multifunction electrode for external defibrillation, pacing, cardioversion, and monitoring. The device is non-sterile and for single use only.
FDA Devices Moderate Nov 25, 2015

ECG Electrodes: 50007  Stablebase SBW55 50675  Stablebase SBW55-15 58051  Skintact W-60 50547  Stablebase SBT60 Only OUS: 50476 Skintact W-60HP E3 I 58046 Skintact T-60 I Patz K920 58688 Dahlhausen 1900000440 59629 Cardionetics CN-15-W60 58789 Lessa 99.832.02 58872 EF Medica FS 50 LG 50359Ultragel FS50LG
FDA Devices Moderate Apr 8, 2015

Skintact ECG Electrode FS-50, Catalog no. 58028 , & Stable Base ECG Electrode SBT-60, Catalog no. 50547. To acquire and transmit the electrical signal at the body surface to a processor that produces an electrocardiogram (ECG) or vectorcardiogram.

Leonhard Lang Medizintechni… is a small archive contributor

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 (4 here).

1 Epic, LLC 4 3rd Day Beverages LLC 4 A.p. Deauville, LLC 4 Aaa Pharmaceutical, Inc. 4 Ab Sciex, LLC 4

Similar medical devices volume

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

Ab Sciex, LLC 4 Accelerate Diagnostics Inc 4 Accord Media, LLC 4 Accumetrics Inc 4

Frequently Asked Questions

How many federal recall notices name Leonhard Lang Medizintechni…? ▼
PlainRecalls indexes 4 distinct federal recall events naming Leonhard Lang Medizintechnik 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 Leonhard Lang Medizintechni… sit among other recalling firms? ▼
Leonhard Lang Medizintechnik GmbH ranks #3,009 of 14,151 by distinct recall-event count among 14,151 firms in this archive (77th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Leonhard Lang Medizintechni…'s notices? ▼
FDA Devices accounts for 4 of this firm's 4 indexed notices.
What product category dominates Leonhard Lang Medizintechni…'s filing book? ▼
Filings for Leonhard Lang Medizintechnik 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.
Leonhard Lang Medizintechnik GmbH: 4 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 Leonhard Lang Medizintechnik GmbH; individual notices remain authoritative on each linked recall page.

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