Recall Atlas
Drugs & medicalClass I

Mercury Enterprises, Inc. dba Mercury Medical recalls Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809,…

Gas powered emergency resuscitator has a circuit flow controller manufactured with an undersized spring, which may cause resuscitator not reach the high and low ends of the PIP and PEEP pressure ranges, which may cause…

Read the official notice →
Date
2025-01-22
Country
United States
Brand
Mercury Enterprises, Inc. dba Mercury Medical
Product
Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810, 1050811, 1050814,…
Classification
Class I
Units
Worldwide Distribution: US (nationwide) to states of: PA, FL, IN, WI, ME, SC,…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Mercury Enterprises, Inc. dba Mercury Medical recalls

  1. 2024-10-09
  2. US
    Drugs & medicalClass I

    Mercury Enterprises, Inc. dba Mercury Medical recalls Neo-Tee T-Piece Resuscitator. Part Numbers 1050805, 1050832. For pediatric emergency respiratory support.

    Manual resuscitator circuit flow controller may come apart due to a missing manufacturing step.

    FDA · DeviceMercury Enterprises, Inc. dba Mercury MedicalUS distribution to MI, FL, SC, PA, IN. International distribution to Albania.Official notice →
All 2 Mercury Enterprises, Inc. dba Mercury Medical recalls →

Other drugs & medical recalls in the United States

  1. 2025-01-22
  2. US
    Drugs & medicalClass I

    Nuwellis Inc recalls nuwellis AquaFlexFlow UF 500 Plus, REF 114156, Catalog Number A06163, extracorporeal blood circuit which is used with the Aquadex…

    The AquaFlexFlow UF 500 Plus extracorporeal blood circuit used with the Aquadex SmartFlow and FlexFlow Systems may indicate "Ultrafiltrate Weight Mismatch" or Excessive Weight Mismatch Alarms while in use. If not…

    FDA · DeviceNuwellis IncUS Nationwide Distribution and the country of Hong KongOfficial notice →
  3. US
    Drugs & medicalClass I

    Abiomed, Inc. recalls Impella RP Flex with SmartAssist; Product Number: 1000323;

    Optical Sensors have been damaged due to physical interaction between the inlet and another device resulting in a Placement Signal Not Reliable (PSNR) alarm and loss of Central Venous (CV) Placement Signal, Pulmonary…

    FDA · DeviceAbiomed, Inc.Domestic: Nationwide Distribution International: CanadaOfficial notice →
  4. US
    Drugs & medicalClass I

    Boston Scientific Corporation recalls PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL MRI (Model Number L211), EL (Model Number L221),…

    A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry or other normal, higher-power operations due to…

    FDA · DeviceBoston Scientific CorporationUS (Nationwide) including Puerto Rico and US Virgin Islands and OUS (foreign)…Official notice →
  5. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline Fluid Delivery Set with Drip Chamber: 1) MTO,135,YELLOW,MICRO,SPK-MAIMONIDES, Item Number: 60130527; 2)…

    Fluid Delivery Sets were incorrectly assembled with a white macro drip chamber instead of the required grey micro drip chamber. The macro drip chamber delivers three times more fluid per drop than the micro drip chamber.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide DistributionOfficial notice →
  6. US
    Drugs & medicalClass I

    Trokamed GmbH recalls Sheath, 18 Fr., 130 mm (REF: WA2PS18S), gastroenterology-urology endoscopic access overtube.

    If the inflow speed is too quick, it could result in reduced outflow through the shaft due to blood, tissue fragments and kidney stone fragments, and quickly build up of intrarenal pressure.

    FDA · DeviceTrokamed GmbHUS (Domestic) distribution in state of PA and OUS (foreign) to country of…Official notice →
  7. US
    Drugs & medicalClass II

    Viatris Inc recalls Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV…

    Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.

    FDA · DrugViatris IncUSA nationwide.Official notice →
See all drugs & medical recalls →