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Injection Needle, REF: 25207 recallZ-0571-2024 · Karl Storz Endoscopy · initiated Oct 24, 2023

Open, Classified

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Karl Storz Endoscopy or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

The efficacy of the manual cleaning process cannot be assured for the affected injection needles intended for general surgery and visceral surgery, which if used, may expose the patient to a higher risk of infection.

FDA root cause category: Device Design

What the company is doing

On 10/24/23, recall notices were mailed to representatives for medical product safety, users, operators, distributors who were asked to do the following: 1) Discontinue use of all affected Injection Needles. 2) Pass on the Recall Notice to all users of the affected products and all other persons who need to be aware within your organization. 3) If you have or may have distributed the products listed, please identify and promptly notify those recipients, or provide the recalling firm with a list of customers who received/may have received the products listed. 4) Contact Customer Support to arrange for the return of affected devices by calling 800-421-0837. 5) Return the completed Customer Reply Form via email to [email protected] For all other questions regarding this communication, please send an email to [email protected]

Recall details

Recall number
Z-0571-2024
Status
Open, Classified
Initiated by the company
Oct 24, 2023
Posted by the FDA
Dec 18, 2023
Recalling firm
Karl Storz Endoscopy
Quantity
1
Product code
GCF
FDA submissions
K945209
Distribution
US: MI, NH, SC, PA, FL, NY, NC, MS, MO, CA, NJ, IL, NV, OK, CO, OH, WA, WI, VA, IN, IA, AR, TX, WV, MD, MN, GA, MA, NM, VT, AK, OR, ID, LA, KS, DC, KY, HI OUS: Mexica, Canada, Germany

Product description

Injection Needle, REF: 25207

Code information (models, lots, serial numbers)

UDI-DI: 04048551085776. All lot numbers

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

Other products in the same recall event

The FDA groups related products into one recall event (event 93328).

Sources and updates

How recalls are matched to devices · Editorial policy · Report an error on this page