Clinical Innovations, LLC
6 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (6)
Registered facilities (1)
- CLINICAL INNOVATIONS, LLC FEI 1000220650 · UT
Recalls & enforcement
- Class IIOngoing2026-03-09Due to complaints of device breakage at the traction force gauge to handle joint.
- Class IITerminated2020-08-13Possible 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 ha…
- Class IITerminated2019-08-06There is a potential for loss of vacuum or failure to generate vacuum when using the firm's fetal vacuum delivery system.
- Class IITerminated2019-05-30An 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 …
- Class IITerminated2015-01-05Clinical 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.
- Class IITerminated2014-12-30Potential for a balloon leak in all lots of (CTS-1000) manufactured since August 2014.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Clinical Innovations, LLC — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10035300-clinical-innovations-llc/
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