Recall Z-1474-2024— Karl Storz Endoscopy

Class II · Ongoing

Class II FDA medical device recall by Karl Storz Endoscopy, initiated 2024-02-27. FDA's recall record names no specific 510(k) clearance for this event. Product: Karl Storz SE & CO. KG, REF 723014, Uvula Retractor, For Veterinary Use Only, Rx Only. Reason: Inadequate reprocessing validation evidence.

Recalling firm
Karl Storz Endoscopy
Classification
Class II
Status
Ongoing
Initiated
2024-02-27
Firm location
El Segundo, CA, United States

Product description

Karl Storz SE & CO. KG, REF 723014, Uvula Retractor, For Veterinary Use Only, Rx Only

Reason for recall

Inadequate reprocessing validation evidence

Data sourced from openFDA. This site is unofficial and independent of the FDA.