Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open… — Class II medical device recall Z-0147-2015
Terminated recall by CooperSurgical, Inc. D.B.A. Lone Star Medical Products, reported 2014-11-05, distributed nationwide. CooperSurgical is recalling two lots of 900-863 because the wrong package insert (IFU) was placed into the shi
| Recall number | Z-0147-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc. D.B.A. Lone Star Medical Products, Stafford, TX, United States |
| Recall initiated | 2013-09-13 |
| Classified | 2014-10-29 |
| Reported by FDA | 2014-11-05 |
| Terminated | 2015-09-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, IT |
| Quantity | 90 units |
| Lot numbers | 149460, 149911 |
Product
Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy.
Reason for recall
CooperSurgical is recalling two lots of 900-863 because the wrong package insert (IFU) was placed into the shipper.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0147-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.