Pilling Modular Verres Body/Obturator, Product Code 140880
This recall has been terminated (originally issued March 16, 2016).
- Company
- Teleflex Medical
- Recall Initiated
- January 8, 2015
- Posted
- March 16, 2016
- Terminated
- April 14, 2017
- Recall Number
- Z-1178-2016
- Quantity
- 8
- Firm Location
- Research Triangle Park, NC
- Official Source
- View on FDA website ↗
Reason for Recall
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).
Distribution
US Distribution to the state of : UT
Lot / Code Info
Lot K3
Root Cause
Packaging process control
Action Taken
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.