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Medline HCSPUPPYRecalls & reported problems

Medline Industries, Inc. · COMPRESSOR,NEBULIZER, CHARACTER, PUPPY · Class 2

Quick summary

This Medline puppy nebulizer compressor is a portable air compressor for nebulizer treatments. Reports mostly describe weak, blocked or no airflow that makes treatments take much longer, along with unusual noise, and mention cough and breathing difficulty in a few cases. There are 23 reports naming its identifier, with no deaths and 2 injuries, and no recalls name this device. There were 19 reports in the recent period compared with 2 in the prior period.

AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.

Adverse event reports
15
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00888277678166), received between Jan 11, 2024 and Sep 29, 2026 — classified as 2 injuries, 13 malfunctions.

The most frequently reported specific device problem is “Infusion or Flow Problem” (7 reports).

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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 1 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 1 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 1 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 1 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 1 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 1 reportsMar 2026: 1 reportsApr 2026: 0 reportsMay 2026: 1 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 7 reportsOct 2026: 0 reports2024202520267
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Infusion or Flow Problem7
  • Restricted Flow rate2
  • Break1
  • Failure to Deliver1
  • Increase in Pressure1
  • Mechanical Problem1
  • No Pressure1
  • Noise, Audible1

Patient problems

  • No Clinical Signs, Symptoms or Conditions13
  • Cough2
  • Bronchitis1
  • Dyspnea1

Recent adverse event reports

The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 29, 2026No Pressure

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50933368 ↗
  • MalfunctionSep 29, 2026Failure to Deliver; Temperature Problem

    It was reported that "The attached neb is getting too hot and not dispensing medicine."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50931510 ↗
  • MalfunctionSep 28, 2026Infusion or Flow Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50917226 ↗
  • MalfunctionSep 25, 2026Break

    It was reported that "ITEM IS BROKEN" and "TOP OF PRODUCT IS BROKEN ADN CAN NOT PUT MED INSIDE."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50899025 ↗
  • MalfunctionSep 25, 2026Infusion or Flow Problem

    It was reported that "The item is no longer misting. She states the item is turning on though."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50898871 ↗
  • MalfunctionSep 18, 2026Restricted Flow rate; Mechanical Problem; Increase in Pressure

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50821148 ↗
  • MalfunctionSep 17, 2026Output below Specifications; Noise, Audible

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50809806 ↗
  • MalfunctionMay 5, 2026Infusion or Flow Problem

    PER CUSTOMER, "WE ARE REQUESTING A CREDIT (NOT REPLACEMENT) FOR 1 DEFECTIVE NEB. ITEM #HCSPUPPY FROM LOT 6462110. SERIAL # (B)(6). THIS UNIT WILL NOT STAY POWERED ON. FD6369767."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25082883 ↗
  • MalfunctionMar 11, 2026Restricted Flow rate

    ACCORDING TO THE CUSTOMER CONTACT, "NEBULIZER TAKES AN HOUR TO MIST AND TO GET THROUGH A TREATMENT FOR HER YOUNG CHILD." THE CUSTOMER CONTACT STATED HER DAUGHTER "MISSED TREATMENT" AS A RESULT OF THE NEBULIZER "NOT PROPERLY MISTING."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24575354 ↗
  • MalfunctionFeb 6, 2026Infusion or Flow Problem

    ACCORDING TO THE CUSTOMER ON 01/04/2026, THE "MACHINE TURNS ON BUT IS NO LONGER MISTING."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24280798 ↗
  • MalfunctionNov 7, 2025Pressure Problem; Pressure Problem

    DEVICE NOT DISPENSING MEDICATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23496460 ↗
  • MalfunctionMar 3, 2025Infusion or Flow Problem; Infusion or Flow Problem

    MACHINE "NOT PUTTING OUT ANY MIST".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21509632 ↗
  • InjuryDec 10, 2024Infusion or Flow Problem; Infusion or Flow Problem

    ACCORDING TO THE CUSTOMER, "A FEW WEEKS AGO" THE NEBULIZER STARTED TURNING ON BUT NOT DISPENSING THE "ALBUTEROL" MEDICATION TO HER SON.

    Patient problems: Bronchitis; Cough; Dyspnea

    MAUDE report 20892956 ↗
  • InjuryJul 24, 2024Infusion or Flow Problem; Infusion or Flow Problem

    ACCORDING TO THE CUSTOMER, ON (B)(6) 2024 THE NEBULIZER "STOPPED MISTING" THE "ALBUTEROL" MEDICATION CAUSING HER DAUGHTER TO DEVELOP A "CONGESTIVE COUGH".

    Patient problems: Cough

    MAUDE report 19822385 ↗
  • MalfunctionJan 11, 2024Smoking; Smoking

    "SMOKING" WHEN TURNED ON

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18498189 ↗

Other Compressor, air, portable devices

All Compressor, air, portable devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.