Medline Industries, Inc. DYNJ901205CRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889942580606), received between Oct 18, 2021 and Oct 18, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Expiration Date Error” (2 reports).

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 18, 2026.

Recalls naming this device

1. Oct 27, 2021Class IITerminated

   NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after 04/2020.

   Z-0358-2022 · Root cause: Incorrect or no expiration date · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryOct 18, 2021Expiration Date Error

  IT WAS REPORTED THAT EXPIRED 0.9% SODIUM CHLORIDE IN THE EVLP PACK WAS USED IN CLINICAL PROCEDURES FOR LUNGS THAT WERE TRANSPLANTED INTO A PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12647862 ↗
• InjuryOct 18, 2021Expiration Date Error

  IT WAS REPORTED THAT EXPIRED 0.9% SODIUM CHLORIDE IN THE EVLP PACK WAS USED IN CLINICAL PROCEDURES FOR LUNGS THAT WERE TRANSPLANTED INTO A PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12647364 ↗