Pilling Modular Verres Body/Obturator, Product Code 140880
Reported: March 23, 2016 Initiated: January 8, 2015 #Z-1178-2016
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).
Details
- Recalling Firm
- Teleflex Medical
- Units Affected
- 8
- Distribution
- US Distribution to the state of : UT
- Location
- Research Triangle Park, NC
Frequently Asked Questions
What product was recalled? ▼
Pilling Modular Verres Body/Obturator, Product Code 140880. Recalled by Teleflex Medical. Units affected: 8.
Why was this product recalled? ▼
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).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 23, 2016. Severity: Moderate. Recall number: Z-1178-2016.
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