Recall Z-1178-2016— Teleflex Medical
Class II · Terminated
Class II FDA medical device recall by Teleflex Medical, initiated 2015-01-08, terminated 2017-04-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Pilling Modular Verres Body/Obturator, Product Code 140880. 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)..
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-01-08
- Terminated
- 2017-04-14
- Firm location
- Research Triangle Park, NC, United States
Product description
Pilling Modular Verres Body/Obturator, Product Code 140880
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).
Data sourced from openFDA. This site is unofficial and independent of the FDA.