Regard™ LD00199PRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10194717110156), received between Jun 17, 2022 and Jun 17, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Delivered as Unsterile Product” (1 report).

1 FDA recall record name this device's identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

1. Jun 3, 2022Terminated

   Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.

   Z-1408-2022 · Root cause: Process change control · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 17, 2022Delivered as Unsterile Product; Packaging Problem

  A NON-STERILE 10ML SYRINGE WAS ADDED TO THIS KIT AS A SUB ITEM IN PLACE OF THE STERILE VERSION OF THE COMPONENT. THIS KIT IS NOT STERILIZED PRIOR TO DISTRIBUTION, SO THE KIT CONTENTS ARE REQUIRED TO BE STERILE PRIOR TO ADDING TO THE KIT. THE 10 ML SYRINGE IS REQUIRED TO BE STERILE FOR USE, BUT WAS DISTRIBUTED TO THE DIRECT ACCOUNT AS NON-STERILE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14735308 ↗