ChemoLock Close Vial Spike REF CL-80 The Chemolock Closed System Transfer Device prevents the transfer of environmental contaminants. The Chemolock is needle free and cannot be deactivated, which will passively aid in preventing needlestick injuries and the exposure to cytotoxic medications for healthcare personnel.
Recall
- Recall Number
- Z-0652-2025
- Event Number
- 95649
- Firm
- ICU Medical, Inc.
- FEI Number
- 2025816
- Product Code
- ONB
- Status
- Open, Classified
- Root Cause
- Packaging process control
- Initiated
- November 6, 2024
- Posted
- December 9, 2024
- Address
- 951 Calle, Amanecer San Clemente, CA, 92673-6212
Description
ChemoLock Close Vial Spike REF CL-80 The Chemolock Closed System Transfer Device prevents the transfer of environmental contaminants. The Chemolock is needle free and cannot be deactivated, which will passively aid in preventing needlestick injuries and the exposure to cytotoxic medications for healthcare personnel.
Due to finished goods incorrectly packaged and labeled.
On 11/06/2024, the firm send an "URGENT Medical Device Correction" Letter via third party (Sedgwick, Inc.) to customers informing them that product was incorrectly packaged and labeled. Product CL-80 package incorrectly contained product code CL-80S. The CL-80 is a used with a 20 mm or a 28 mm vial where as CL-80S is only use for a 20 mm vial. The issue is using the incorrect adapter may result in leakages. Actions to be taken by the Customer: Discontinue use mislabeled lot 13953938 of CL-80 and discard remaining product from this specific lot. 1. Check all inventory locations within your institution for the affected product listed in the notification and discontinue use. Quarantine and destroy all affected products following your institution s process for destruction. If destroying is not immediately possible at your facility, then the product should be quarantined until disposal. 2. Share this notification with all potential users of the device to ensure they are aware of this notification. If the devices are used at another location, please ensure this communication is delivered there./// 3. Complete and return the attached Customer Response Form to [email protected] within 10 days of receipt to acknowledge your understanding of this notification./ / 4. DISTRIBUTORS: If you have distributed affected products to your customers, please immediately forward this notice to them. Request that they complete the response form and return it to [email protected]. For questions/assistance, contact: Global Complaint Management 1-844-654-7780 (M-F, 8:00am 5:00pm CT) or [email protected] To report adverse events or product complaints Customer Service 1-866-829-9025, option 8 or [email protected] (M-F, 8:00 am 6:00 pm CT) Additional information or to request a credit. Field Action Processing 1-888-843-0245 [email protected] Questions about this communication
Worldwide - U.S. Nationwide distribution in the state of IL and the country of Canada.
6000 units