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n.a.

Karl Storz GmbH & Co. KG · Model 11001KL · UDI-DI 04048551049853

EOQ Prescription
10
510(k) clearances
31,113
Adverse events (204 deaths)
160
Recalls
189
Facilities

Description

Biopsy Forceps, 1.8 mm

Recalls

DateFirmReason
2026-01-29Olympus Corporation of the AmericasPotential for rubber fragment detachment during use.
2026-01-29Olympus Corporation of the AmericasPotential for rubber fragment detachment during use.
2026-01-21Auris Health, IncDevice for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope loading, application w
2025-12-04Intuitive Surgical, Inc.Due to probe bags that may have a compromised or incomplete sterile pouch seal.
2025-09-12Noah Medical CorporationDue to Users not having access to the Instructions for Use/User Manual due to it being password protected.
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.