Cooper Surgical TAMPA CATHETER 5 French 33 cm — Class II medical device recall Z-1782-2014
Terminated recall by CooperSurgical, Inc., reported 2014-06-18, distributed nationwide. Sterility of the device may be compromised due to unsealed pouch
| Recall number | Z-1782-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc., Trumbull, CT, United States |
| Recall initiated | 2014-05-13 |
| Classified | 2014-06-11 |
| Reported by FDA | 2014-06-18 |
| Terminated | 2015-05-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 1,180 units |
| Reason classes | sterility |
| Lot numbers | 141525 |
| Model numbers | 61-2005 |
Product
Cooper Surgical TAMPA CATHETER 5 French 33 cm. Intended for Hysterosonography. Model Number: 61-2005
Reason for recall
Sterility of the device may be compromised due to unsealed pouch
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-1782-2014. 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.