Ally Uterine Positioning System — Class II medical device recall Z-1727-2015
Terminated recall by CooperSurgical, Inc., reported 2015-06-17, distributed in CA, IL, NC, NY. Design of device may expose user to injury to fingers or body parts
| Recall number | Z-1727-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc., Trumbull, CT, United States |
| Recall initiated | 2015-05-18 |
| Classified | 2015-06-08 |
| Reported by FDA | 2015-06-17 |
| Terminated | 2015-08-07 |
| Distributed | CA, IL, NC, NY |
| Quantity | 5 units |
| Serial numbers | 020015, 020021, 020023, 020043, 020051 |
Product
Ally Uterine Positioning System (Ally UPS) used in the mounting and positioning and holding of uterine manipulators during gynecological laproscopic procedures Model: Ally UPS
Reason for recall
Design of device may expose user to injury to fingers or body parts
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-1727-2015. 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.