Z-1727-2015 Class II Terminated
FDA device recall Z-1727-2015 was initiated by CooperSurgical, Inc. on May 18, 2015 and is designated Class II. Reason for recall: Design of device may expose user to injury to fingers or body parts The recall status is terminated (terminated Aug 7, 2015). Affected quantity: 5 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 17, 2015
- Initiation Date
- May 18, 2015
- Termination Date
- Aug 7, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5 units
Product Description
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
Distribution Pattern
Distributed in the states of CA, IL, NC, and NY.
Code Information
Serial Numbers: 020015;020021;020023; 020043;020051
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1727-2015
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026