CooperSurgical H/S CATHETER — Class II medical device recall Z-2570-2014
Terminated recall by CooperSurgical, Inc., reported 2014-09-17, distributed in CA, CO, DC, FL, GA, HI, ID, IL…. Unsealed pouches.
| Recall number | Z-2570-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc., Trumbull, CT, United States |
| Recall initiated | 2014-07-03 |
| Classified | 2014-09-05 |
| Reported by FDA | 2014-09-17 |
| Terminated | 2015-05-28 |
| Distributed | CA, CO, DC, FL, GA, HI, ID, IL, MD, MI, MS, NC, NJ, NY, OR, PA, TX, WA |
| Countries outside the US | ES, GB, NL |
| Quantity | 1,400 units |
| Lot numbers | 153914 |
| Model numbers | 61-5007 |
Product
CooperSurgical H/S CATHETER (PART # 61-5007) Intended for Hysterosonography/ Hysterosalpingography.
Reason for recall
Unsealed pouches.
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-2570-2014. 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.