PlainRecalls

Karl Storz Endoscopy America Inc

Compiled from official public sources by the publisher.

17 recalls on record · Latest: Dec 25, 2013

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Agency notice ledger

Federal filing book Karl Storz Endoscopy Americ… LIGHT-BOOK · SINGLE-AGENCY

#933 of 14,151 · 17 notices · 0.016% archive

  • BOOK 17 notices
  • RANK #933 of 14,151
  • SHARE 0.016% archive
  • AGENCY FDA Devices (17)
  • CAT medical devices
  • CATS 1 category
  • LATEST Dec 25, 2013
  • PHOTO Actavis Inc

Nearest notice-volume peer: Actavis Inc (0 notice gap)

Karl Storz Endoscopy America Inc accounts for about 0.016% of the 104,423-notice archive on 17 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Karl Storz Endoscopy Americ…'s standing among 14,151 recalling firms

Karl Storz Endoscopy America Inc ranks 933rd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Karl Storz Endoscopy Americ… vs all firms by recall-notice count

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

17 933rd of 14151 higher than 13,196 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

Karl Storz Endoscopy Americ… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Karl Storz Endoscopy America Inc holds about 0.016% of archive notices alongside 17 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Dec 25, 2013

Broncho Flexible Fiberscope, models: 11001BN1, 11002BD1, 11004BC1, and 11009BC1. " Examination and treatment of the tracheobronchial tree Contraindications for Bronchoscopy " Uncontrolled angina, uncontrolled heart failure, or serious uncontrolled ventricular arrhythmias " Uncontrolled hypertension " Bleeding disorder or use of anticoagulants.
FDA Devices Moderate Dec 25, 2013

Intubation Flexible Fiberscope, Models: 11301AA1, 11301BN1, 11302BD1, 11302BD2, 11304BC1, 11340BC1, 11301BND1, 11302BDD1, and 11302BDD2. " Transoral intubation " Transnasal intubation " Evaluation of placement of endotracheal and double lumen endotracheal tubes " Provide visual access to the larynx and tracheobronchial tree.
FDA Devices Moderate Dec 18, 2013

Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey forceps to grasp tissue.
FDA Devices Moderate Jul 24, 2013

27023WU Balloon Catheter, 3 Fr., 2/pkg, sterile, contains latex. The RUSCH ureter occlusion catheter is indicated for the routine occlusion of the ureter to prevent the movement of stone fragments during treatment. The coaxial catheters will also allow simultaneous drainage of urine or infusion of other solutions.
FDA Devices Moderate May 22, 2013

Electrode, cutting, 24FR (27050G/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Electrode, Roller, Vaporization, 24FR (27050RK/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Electrode, Roller Ball, 24FR (27050NK/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Electrode, Coag, Pointed, 24FR (27050L/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Electrode, Cutting, 24FR, 0.30MM (27040G-.30/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Electrode, VaporCut, 24FR (27050SG/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Loop, Cutting, Angled 22FR (26055G/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Knife, Cold, Straight (27068K/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Electrode, cutting, 24FR (27050G-.30/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Electrode, Coag, Ball End, 24FR (27050N/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Loop, Cutting, 24FR (26050G/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 22, 2013

Electrode, Barrel Bar, 24FR (27050NX/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Devices Moderate May 15, 2013

KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System, Instruction Manuals: PDD Telescopes, Tricam SL II, and PDD Camera Heads. Used as an optional accessory to white light cystoscopy when used in combination with the diagnostic imaging drug Cysview.

Karl Storz Endoscopy Americ… holds a measurable archive slice

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

Similar medical devices volume

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

Ad-Tech Medical Instrument Corporation 17 Fhc, Inc. 17 Ge Healthcare It 17 Hitachi Medical Systems America Inc 17

Frequently Asked Questions

How many federal recall notices name Karl Storz Endoscopy Americ…? ▼
PlainRecalls indexes 17 distinct federal recall events naming Karl Storz Endoscopy America 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 Karl Storz Endoscopy Americ… sit among other recalling firms? ▼
Karl Storz Endoscopy America Inc ranks #933 of 14,151 by distinct recall-event count among 14,151 firms in this archive (93rd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Karl Storz Endoscopy Americ…'s notices? ▼
FDA Devices accounts for 17 of this firm's 17 indexed notices.
What product category dominates Karl Storz Endoscopy Americ…'s filing book? ▼
Filings for Karl Storz Endoscopy America 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.
Karl Storz Endoscopy America Inc: 17 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 Karl Storz Endoscopy America Inc; individual notices remain authoritative on each linked recall page.

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