FDA Device recall Z-2570-2014
CooperSurgical H/S CATHETER (PART # 61-5007) Intended for Hysterosonography/ Hysterosalpingography
- FDA Device
- Class II
- terminated
- Published 2014-09-17
On 2014-09-17 the FDA classified a Class II recall of CooperSurgical H/S CATHETER (PART # 61-5007) Intended for Hysterosonography/ Hysterosalpingography by Coopersurgical, citing unsealed pouches.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2570-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-07-03 |
| Published | 2014-09-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Coopersurgical |
| Distribution | CA, CO, DC, FL, GA, HI, ID, IL, MD, MI, MS, NC, NJ, NY, OR, PA, TX, WA |
Product
CooperSurgical H/S CATHETER (PART # 61-5007) Intended for Hysterosonography/ Hysterosalpingography.
Reason
Unsealed pouches.
Identifiers
| code_info | Lot 153914 |
|---|
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-2570-2014%22
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