FDA Recall Terminated

4Fr x 20cm Single Lumen CT Midline Basic Tray, Product Code: VYML4S1001

Recall: Z-0585-2020 · Initiated September 24, 2019

Recall

Recall Number
Z-0585-2020
Event Number
84010
Firm
Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.
FEI Number
1000120555
Product Code
PND
Status
Terminated
Root Cause
Packaging process control
Initiated
September 24, 2019
Terminated
October 21, 2020
Address
87 Venture Dr, Dover, NH, 03820-5914

Description

4Fr x 20cm Single Lumen CT Midline Basic Tray, Product Code: VYML4S1001

Reason

Potential that 3Fr size catheter placed in the catheter tray instead of 4Fr for the 4Fr x 20cm Single Lumen CT Midline Basic Tray.

Action

On September 25, 2019 the firm distributed Urgent Medical Device Recall Communication letters by e-mail instructing them to: 1. Check your stock for the products included within the scope of the recall. Immediately cease use and distribution, and quarantine all affected product immediately. 2. Count and document your affected inventory on the Recall Acknowledgement and Inventory Return Form in Attachment 1. Please complete and return the document even if you currently have no product on hand. 3. Fax or email the form to Vygon including customer contact information. 4. Vygon customer service will contact the customer and issue a Return Merchandise Authorization number. 5. Return the product as well as the original signed Recall Acknowledgement and Inventory Return Form using the instructions from Customer Service involving product pick-up. 6. All inventory will be credited or replaced at no cost to you. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDAs MedWatch Adverse Event Reporting program either online, by regular mail or by fax. If you have any questions, please contact your local sales representative or Vygons Customer Service Department at 1-800-473-5414 Monday-Friday 8am 6pm, or by e-mail at [email protected].

Distribution

One Customer Located in TN

Quantity

75