Recall Z-1178-2016 ยท GDM Needle, Aspiration And Injection, Reusable
Teleflex Medical
Pilling Modular Verres Body/Obturator, Product Code 140880
| Date | Mar 16, 2016 (initiated Jan 8, 2015) |
| Status | Terminated |
| Reason | Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip). |
| Root cause | Packaging process control |
| Action | Teleflex sent an Medical Device Advisory Notification letter dated January 8, 2016, to all affected customers notifying them of the packaging error. Our records indicate that you have received products that are subject to this notification. Teleflex Medical is committed to providing high quality, safe and effective products. We sincerely apologize for any inconvenience this action may cause your operations. If you have any other questions, feel free to contact your local sales representative or Customer Service at recalls@teleflex.com or 1-866-246-6990. |
| Quantity | 8 |
| Distribution | US Distribution to the state of : UT |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.