FDA Device recall Z-0147-2015
Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy
- FDA Device
- Class II
- terminated
- Published 2014-11-05
On 2014-11-05 the FDA classified a Class II recall of Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy by Coopersurgical D B A Lone Star Medical Products, citing cooperSurgical is recalling two lots of 900-863 because the wrong package insert (IFU) was placed into the shipper.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0147-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-13 |
| Published | 2014-11-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Coopersurgical D B A Lone Star Medical Products |
| Distribution | US |
Product
Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy.
Reason
CooperSurgical is recalling two lots of 900-863 because the wrong package insert (IFU) was placed into the shipper.
Identifiers
| code_info | Lots 149460 and 149911 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0147-2015%22
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