Cook Vacuum Pump — Class II medical device recall Z-1460-2018
Terminated recall by Cook Inc., reported 2018-04-25. Pump was found to be constructed from crimp connectors that do not meet the fixation wiring requirements and c
| Recall number | Z-1460-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cook Inc., Bloomington, IN, United States |
| Recall initiated | 2018-03-22 |
| Classified | 2018-04-19 |
| Reported by FDA | 2018-04-25 |
| Terminated | 2020-05-13 |
| Countries outside the US | AR, BO, BR, CA, CO, GT, MX, PA, PE, UY, VE |
| Quantity | 132 |
Product
Cook Vacuum Pump (Cook Aspiration Unit) K-MAR-5200-US, GPN G51607. Intended for the aspiration of body fluids and cells; in particular oocyte aspiration.
Reason for recall
Pump was found to be constructed from crimp connectors that do not meet the fixation wiring requirements and can cause failure of the device to operate or electric shock or burn to the user.
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-1460-2018. 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.