Recall Z-1530-2020

Karl Storz Endoscopy · initiated August 27, 2019

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible Pediatric Neuroscope

Codes / lots: All Lots

Reason for recall

During a complaint investigation it was determined that an error was observed within the instruction manual included with some scopes. Specifically, The Quick Connector Kits (QCK) and tray information, specified for the STERIS System 1E (SS1E) sterilization method within the instruction manual is incorrect. If the user uses SS1E to sterilize the impacted scopes and referred to the manual concerning the QCK information, the sterility of reprocessed scope cannot be guaranteed.

FDA-determined cause: Error in labeling

Action taken

On 8/27/2019 the firm sent an "Urgent Medical Device - Correction" letter detailing the recall was mailed to consignees. In addition to addressing the recall it asked customers to do the following: 1. If you use STERIS SS1E to sterilize the above scopes, and if you selected the specific QCK and tray according to the KARL STORZ Instruction Manuals, please be aware that the sterility of the scope cannot be guaranteed and that you should consider taking necessary actions to address any patient safety concerns. 2. Other than STERIS SS1E system, these scopes can also be sterilized via EtO, STERRAD Systems (NX, 100S and 100NX), V. PRO maX and V. PRO 60. If you use any of these sterilization methods, the QCK error should have no safety impact to your patients. 3. If you have experienced any adverse event with the above scopes, please let us know and at the same time, follow the FDAs MedWatch Adverse Event Reporting process at: https://www.fda.gov/medical-devices/medical-device-safety/medical-device-reporting-mdr-how-report-medical-device-problems#voluntary 4. Attached with this letter we are providing you a copy of the newly revised Instruction Manual for the scope(s) you have received. They are: -11005BC1 Flexible Bronchoscope Print Control #Z21493US-BA -11161C2 Flexible Neuroscope Print Control #Z21491US-BA -11282BN1 Flexible Pediatric Neuroscope Print Control #Z21491US-BA 5. Please be sure to use only the above listed manuals and discard all others. If you would like to receive additional copies, please contact our Technical Support at 800-421-0837, Ext. 5350. If you have any patient safety questions please do not hesitate to contact our Chief Medical Officer, Dr. Dennis Fowler, at 424-218-8603.

Details

Recall number
Z-1530-2020
Initiated
August 27, 2019
Product code
GWG – Endoscope, Neurological
Quantity
73 scopes
Distribution
US: AL, AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, MD, MI, MN, MO, NC, NH, NJ, OH, OR, PA, SC, TN, TX, VA, WA, WI, WV, OUS: Canda
Recalling firm
Karl Storz Endoscopy, El Segundo, CA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-1531-2020 Class IIKarl Storz, Model # 11161C2, Flexible NeuroscopeDuring a complaint investigation it was determined that an error was observed within the instruction manual… 08/27/2019Open, Classified
Z-1532-2020 Class IIKarl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE, Model # 11005BC1During a complaint investigation it was determined that an error was observed within the instruction manual… 08/27/2019Open, Classified