Recall archive
29 recalls · page 2 of 2
Reported Dec 25, 2013
Intubation Flexible Fiberscope, Models: 11301AA1, 11301BN1, 11302BD1, 11302BD2, 11304BC1, 11340BC1, 11301BND1,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy America Inc.
Matched: Brand · Reason for recall — KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho Fiberscope or a Flexible Intubation Fiberscope with a suction port because the…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2013
Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey forceps to grasp…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy America Inc.
Matched: Brand · Reason for recall — KARL STORZ is recalling the Axillent Debakey Grasping Forceps because the 33821WTD Wavy grasper was mislabeled as 33821DYD Axillent Debakey Grasping…
FDA (openFDA device enforcement)
Reported Jul 24, 2013
27023WU Balloon Catheter, 3 Fr., 2/pkg, sterile, contains latex. The RUSCH ureter occlusion catheter is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy America Inc.
Matched: Brand · Reason for recall — Karl Storz Endoscopy-America has initiated the recall of the 27023WU Balloon Catheter because the packaging may be compromised, and therefore the…
FDA (openFDA device enforcement)
Reported May 22, 2013
Electrode, cutting, 24FR (27050G/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy America Inc.
Matched: Brand · Reason for recall — Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination.
11 more products in this recall
FDA (openFDA device enforcement)
Reported May 15, 2013
KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System, Instruction Manuals: PDD Telescopes, Tricam SL II, and PDD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy America Inc.
Matched: Brand · Product · Product details · Reason for recall — The recall was initiated because Karl Storz has confirmed that the Photodynamic Diagnosis (PDD) D-Light C System instruction manuals have important…
FDA (openFDA device enforcement)
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