Karl Storz Endoscopy FIVE S 3.5x65, Flexible Intubation Videoscope, REF: 091361-01 (1 Unit), and 091361-06 (6 Units) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
FIVE S 3.5x65, Flexible Intubation Videoscope, REF: 091361-01 (1 Unit), and 091361-06 (6 Units)
Brand
Karl Storz Endoscopy
Lot Codes / Batch Numbers
All LOTs with remaining shelf life
Products Sold
All LOTs with remaining shelf life
Karl Storz Endoscopy is recalling FIVE S 3.5x65, Flexible Intubation Videoscope, REF: 091361-01 (1 Unit), and 091361-06 (6 Units) due to During a regular requalification review, affected flexible intubation video endoscopes did not achieve the required sterility assurance level. There i. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
During a regular requalification review, affected flexible intubation video endoscopes did not achieve the required sterility assurance level. There is a risk that the patient may be exposed to a higher risk of infection.
Recommended Action
Per FDA guidance
On 09/10/21 recall notices were mailed to customers. Action to be taken by the user 1. Immediately quarantine and discontinue use of the affected products. 2. Pass on this Urgent Field Safety Notice to all users of the products listed above and all other persons who need to be aware within your organization. 3. If you have distributed the affected products to third parties, please promptly forward this letter to the recipients of the products and indicate contact details of the recipient on the Acknowledgement and Response Form. 4. Return the Acknowledgment and Response Form by Fax or E-Mail to the contact listed below within 10 calendar days of receipt of this notice. 5. Get in touch with your KARL STORZ representative to return affected products and to discuss suitable alternative products. This notice must be passed on to all those who need to be aware within your organization or to any organization where the potentially affected devices have been transferred. Complete and return the Customer Acknowledgement and Response Form.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, AR, CA, CO, CT, FL, GA, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, NV, NH, NJ, NM, NY, NC, OH, OR, PA, SC, TN, TX, UT, VT, VA, WA, WV, WI, DC
Page updated: Jan 10, 2026