FDA Medical Device Recalls (openFDA)
CooperSurgical, Inc.: Ally Uterine Positioning System (Ally UPS) used in the mounting and positioning and holding of uterine manipulators during gynecological laproscopic procedures Model: Ally UPS
- Recall number
- Z-1727-2015
- Recalling firm
- CooperSurgical, Inc.
- 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
- Status
- Terminated
- Initiated
- 2015-05-18
- Posted
- 2015-06-08
- Terminated
- 2015-08-07
- Reason
- Design of device may expose user to injury to fingers or body parts
- Root cause
- Device Design
- Action
- CooperSurgical initiated the recall on May 18, 2015 via Fedex with confirmed delivery receipt. The letter identified the affected product and asked users to discontinue use and complete the Acknowledgement and Receipt Form to schedule a replacement. Questions contact 203.601.5200.
- Quantity
- 5 units
- Distribution
- Distributed in the states of CA, IL, NC, and NY.
- Lot, serial or model codes
- Serial Numbers: 020015;020021;020023; 020043;020051
- 510(k) numbers
- ["K141523"]
- PMA numbers
- not on file
- Product code
- LKF
- Firm FEI
- 1216677
- Firm city
- Trumbull
- Firm state
- CT
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28