Karl Storz Endoscopy America recalls
Karl Storz Endoscopy America appears in 17 official U.S. recall notices indexed by RecallRadar, most recently on 2013-12-25.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 17 |
|---|---|
| Published | 2013-05-15 to 2013-12-25 |
| By agency | FDA Device (17) |
| By classification | Class II (17) |
| By status | terminated (17) |
| Distribution named in notices | AZ, FL, IL, IN, TX, US |
Recalls
- Broncho Flexible Fiberscope, models: 11001BN1, 11002BD1, 11004BC1, and 11009BC1. " Examination and treatment of the tracheobronchial tree C…
FDA Device · Class II · 2013-12-25 · Karl Storz Endoscopy America
Reason: KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho Fiberscope or a Flexible Intubation Fiberscope with a suction port because the material used in the suction channel portion was thermoplastic polyuret… - Intubation Flexible Fiberscope, Models: 11301AA1, 11301BN1, 11302BD1, 11302BD2, 11304BC1, 11340BC1, 11301BND1, 11302BDD1, and 11302BDD2. "…
FDA Device · Class II · 2013-12-25 · Karl Storz Endoscopy America
Reason: KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho Fiberscope or a Flexible Intubation Fiberscope with a suction port because the material used in the suction channel portion was thermoplastic polyuret… - Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey forceps to grasp tissue
FDA Device · Class II · 2013-12-18 · Karl Storz Endoscopy America
Reason: KARL STORZ is recalling the Axillent Debakey Grasping Forceps because the 33821WTD Wavy grasper was mislabeled as 33821DYD Axillent Debakey Grasping Forceps. - 27023WU Balloon Catheter, 3 Fr., 2/pkg, sterile, contains latex
FDA Device · Class II · 2013-07-24 · Karl Storz Endoscopy America
Reason: Karl Storz Endoscopy-America has initiated the recall of the 27023WU Balloon Catheter because the packaging may be compromised, and therefore the sterility of the product could be affected. - Knife, Cold, Straight (27068K/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Electrode, Roller Ball, 24FR (27050NK/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Electrode, Barrel Bar, 24FR (27050NX/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Loop, Cutting, Angled 22FR (26055G/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Electrode, Coag, Pointed, 24FR (27050L/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Electrode, Roller, Vaporization, 24FR (27050RK/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Loop, Cutting, 24FR (26050G/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Electrode, cutting, 24FR (27050G/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Electrode, Coag, Ball End, 24FR (27050N/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Electrode, Cutting, 24FR, 0.30MM (27040G-.30/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Electrode, cutting, 24FR (27050G-.30/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - Electrode, VaporCut, 24FR (27050SG/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
Reason: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination. - KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System, Instruction Manuals: PDD Telescopes, Tricam SL II, and PDD Camera Heads
FDA Device · Class II · 2013-05-15 · Karl Storz Endoscopy America
Reason: The recall was initiated because Karl Storz has confirmed that the Photodynamic Diagnosis (PDD) D-Light C System instruction manuals have important safety-related changes.