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PANPAC MEDICAL CORPORATION · Model UI 4.0 · UDI-DI 04715309125137

LKF Prescription

510(k) clearances

1,788

Adverse events (2 deaths)

Recalls

102

Facilities

Description

Uterine Injectors are double lumen, slightly curved and designed for single use. It was developed to facilitate diagnostic procedures such as Laparoscopy, Minilaps, Salpingoplasties and Fertility Examinations. It is a sterile disposable product consisting of plastic tube, connector and other plastic components which meets the USP recommendation for class VI testing.

Recalls

Date	Firm	Reason
2022-05-25	Mckesson Medical-Surgical Inc. Corporate Office	Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 0
2022-03-31	CooperSurgical, Inc.	Incorrect bonding material used for assembly of the catheter, may fail, resulting in detachment of component parts, broken components, or leakage. This breakage may result in delay
2022-03-31	CooperSurgical, Inc.	Incorrect bonding material used for assembly of the catheter, may fail, resulting in detachment of component parts, broken components, or leakage. This breakage may result in delay
2022-03-31	CooperSurgical, Inc.	Incorrect bonding material used for assembly of the catheter, may fail, resulting in detachment of component parts, broken components, or leakage. This breakage may result in delay
2019-05-30	Clinical Innovations, LLC	An incorrect component used during manufacturing. The uterine manipulator tip support does not have the "notch" required to attach the spacer and or colpotomy cup. This may result
2015-05-18	CooperSurgical, Inc.	Design of device may expose user to injury to fingers or body parts
2014-07-03	CooperSurgical, Inc.	Unsealed pouches.
2014-05-13	CooperSurgical, Inc.	Sterility of the device may be compromised due to unsealed pouch
2012-10-31	Cooper Surgical, Inc.	Excessive pressure exerted on the uterine tip when attached to the Arch may, under certain circumstances, cause the internal steel rod of the tip to protrude through the cleaning
2012-10-31	Cooper Surgical, Inc.	Excessive pressure exerted on the uterine tip when attached to the Arch may, under certain circumstances, cause the internal steel rod of the tip to protrude through the cleaning

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.