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Clinical Innovations Recalls
9 recalls on record · February 4, 2015 to May 6, 2026 · Food & Beverage, Medical Devices
Recalls by year
15
20
22
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 6, 2026Medical DevicesFDA
Clinical Innovations, LLC recalls Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number: VAC-60
Hazard: Due to complaints of device breakage at the traction force gauge to handle joint.
September 7, 2022Food & BeverageFDA
Clinical Innovations, LLC recalls Sweetums 24% sucrose solution with preservative. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product
Hazard: Firm received complaints of leaking, black liquid, and black particulates in the product vials.
September 7, 2022Food & BeverageFDA
Clinical Innovations, LLC recalls Sweetums 24% sucrose solution preservative free. Vials containing 1ml or 2ml of 24% sucrose in purified water. Produc
Hazard: Firm received complaints of leaking, black liquid, and black particulates in the product vials.
September 7, 2022Food & BeverageFDA
Clinical Innovations, LLC recalls Sweetums 24% Sucrose Solution Preservative Free 15 mL cups VPSU15037288. Each box contains 288 cups. Product is aseptic
Hazard: Firm received complaints of leaking cups, black liquid, and black particulates in the 24% Sucrose Solution.
December 16, 2020Medical DevicesFDA
Clinical Innovations, LLC recalls Clinical Innovations ROM Plus Collection Kit IFU: ROM Plus Rupture of Membrane Test ROM-5025, ROM-6025
Hazard: Possible false negative or false positive results. The incorrect sample collection swabs (non-scored) were assembled into assembled into the in vitro diagnostic kits. If the user does not break the swab stick correctly, or if scissors or other tools are used to cut the swab handle false negative or false positive results can occur.
June 3, 2020Medical DevicesFDA
Clinical Innovations, LLC recalls Clearview Total Uterine Manipulator (model UM750), The device is labeled in part, "ClearView(R) TOTAL, 7 cm* * *CLINICA
Hazard: 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 in a delay in surgery and additional surgical interventions to completed the procedure. There was a report of an injury.
May 27, 2020Medical DevicesFDA
Clinical Innovations, LLC recalls Kiwi Complete Vacuum Delivery System, Model No. VAC-6000MTE - Product Usage: The Kiwi is a disposable vacuum-assisted fe
Hazard: There is a potential for loss of vacuum or failure to generate vacuum when using the firm's fetal vacuum delivery system.
October 21, 2015Medical DevicesFDA
Clinical Innovations, LLC recalls The Ebb Complete Tamponade System, model #CTS-1000 and Code #OQY. Intended for use in providing temporary control or re
Hazard: Clinical Innovations, LLC is voluntarily recalling the Ebb Complete Tamponade System (CTS-1000) Lot Number 1214-F-403.) to address the potential for a balloon leak which may affect the ability to deliver therapy, when needed.
February 4, 2015Medical DevicesFDA
Clinical Innovations, LLC recalls Ebb Complete Tamponade System, BD-OTS Obstetric Catheter, REF CTS-1000, Rx Only, Sterile EO
Hazard: Potential for a balloon leak in all lots of (CTS-1000) manufactured since August 2014.