PlainRecalls
FDA Devices Moderate Class II Ongoing

Five S 5 3x65, REF: 0915612-06, sterile for single use, Sterile EO, Rx Only

Reported: September 27, 2023 Initiated: July 7, 2023 #Z-2589-2023

Product Description

Five S 5 3x65, REF: 0915612-06, sterile for single use, Sterile EO, Rx Only

Reason for Recall

Flexible intubation endoscopes sterility assurance can not be confirmed.

Details

Recalling Firm
Karl Storz Endoscopy
Units Affected
218 units
Distribution
Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MEX, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV, WY and the country of Canada.
Location
El Segundo, CA

Frequently Asked Questions

What product was recalled?
Five S 5 3x65, REF: 0915612-06, sterile for single use, Sterile EO, Rx Only. Recalled by Karl Storz Endoscopy. Units affected: 218 units.
Why was this product recalled?
Flexible intubation endoscopes sterility assurance can not be confirmed.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 27, 2023. Severity: Moderate. Recall number: Z-2589-2023.