PlainRecalls
FDA Devices Moderate Class II Ongoing

Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only

Reported: April 10, 2024 Initiated: February 27, 2024 #Z-1472-2024

Product Description

Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only

Reason for Recall

Inadequate reprocessing validation evidence

Details

Recalling Firm
Karl Storz Endoscopy
Units Affected
190 units
Distribution
US Nationwide distribution in the states of AR, CA, CO, CT, DC, FL, GA, IA, IL, LA, MA, MI, MN, MO , ND, NY, OH, OR, SD, TN, TX, UT, VA, WA, WV.
Location
El Segundo, CA

Frequently Asked Questions

What product was recalled?
Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only. Recalled by Karl Storz Endoscopy. Units affected: 190 units.
Why was this product recalled?
Inadequate reprocessing validation evidence
Which agency issued this recall?
This recall was issued by the FDA Devices on April 10, 2024. Severity: Moderate. Recall number: Z-1472-2024.