Centurion Medical Products Corporation OR VANTEX 7FR 3L 16CM CVC ECVC6665 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OR VANTEX 7FR 3L 16CM CVC ECVC6665
Brand
Centurion Medical Products Corporation
Lot Codes / Batch Numbers
2018111950 2019031350 2019040550
Products Sold
2018111950 2019031350 2019040550
Centurion Medical Products Corporation is recalling OR VANTEX 7FR 3L 16CM CVC ECVC6665 due to Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of flu. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Recommended Action
Per FDA guidance
On April 24, 2019, the firm notified customers who had received kits containing BD's MaxZero product. Customers were instructed to do the following: 1. Whether or not you have product in inventory, please complete and return the attached Centurion Accountability Record via email- lcarpenter@centurionmp.com or via fax-517-546-3356. 2. Please share this communication with all users of the product within your organization, as directed in the BD letter. 3. Report any adverse health consequences experienced with the use of this product to BD. Events may also be reported to the FDA's MedWatch Adverse Event Reporting program. Web: MedWatch website at www.fda.gov/medwatch Phone: 1-800-FDA-1088 (1- 800-332-1088); Mail: MedWatch, HF-2, FDA, 5600 Fisher's Lane, Rockville, MD 20852- 9787
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