FDA Device recall Z-1178-2016
Pilling Modular Verres Body/Obturator, Product Code 140880
- FDA Device
- Class II
- terminated
- Published 2016-03-23
On 2016-03-23 the FDA classified a Class II recall of Pilling Modular Verres Body/Obturator, Product Code 140880 by Teleflex Medical, citing 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 1408….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1178-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-01-08 |
| Published | 2016-03-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Teleflex Medical |
| Distribution | UT |
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).
Identifiers
| code_info | Lot K3 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1178-2016%22
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