Karl Storz Irrigation Tubing (Karl Storz) – Labeling Error (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Set, Irrigation, PC
Brand
Karl Storz Endoscopy
Lot Codes / Batch Numbers
Product/Material Number: 031523-10 UDI-DI code: 04048438006306 Lot Number: 240222
Products Sold
Product/Material Number: 031523-10 UDI-DI code: 04048438006306 Lot Number: 240222
Karl Storz Endoscopy is recalling Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Set, Irrigation, PC due to Due to improper labeling of products. An intended use on the label has not been reviewed and approved by FDA for distribution in the U.S.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to improper labeling of products. An intended use on the label has not been reviewed and approved by FDA for distribution in the U.S.
Recommended Action
Per FDA guidance
On 10/22/2024, an "URGENT: MEDICAL DEVICE CORRECTION" Letters will be sent via email by KARL STORZ informing customers that the firm has become aware that one lot number of misbranded product was distributed to 19 customers. Customers are instructed to: 1. Pass on this Urgent Medical Device Correction to all users of the products listed above (Table 1) and all other persons who need to be aware within your organization. 2. Communicate to all applicable users that the product is not to be utilized during spinal procedures. 3. If you have or may have distributed the products listed, please identify and promptly notify those recipients of this notice. 4. Return the completed Customer Reply Form by E-Mail to the indicated contact below within 15 calendar days from the date of receipt. 5. Please report any incidents related to this issue to the manufacturer, dealer, or local representative and, if applicable, to the national competent authority, as this is important feedback. for questions send an email to KSEAProductLabeling@karlstorz.com .
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 noticePage updated: Jan 10, 2026