Drugs & medicalClass II

Ohio Medical Corporation recalls Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac…

Increase in premature device failures

Read the official notice →
Date
2022-01-19
Country
United States
Brand
Ohio Medical
Product
Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac…
Classification
Class II
Units
US Nationwide, including PR. There was government and foreign distribution.…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Ohio Medical recalls

  1. 2025-06-25
  2. US
    Drugs & medicalClass II

    Ohio Medical Corporation recalls GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S

    Erroneous calibration values, potentially resulting in: as the device ages, oxygen purity will gradually decrease to the point where the device alarms to indicate low oxygen purity will be incorrect.

    FDA · DeviceOhio Medical CorporationUS Nationwide distribution in the states of AR, FL, VA, ND, MS, MN, CA, NV, KY.Official notice →
All 2 Ohio Medical recalls →

Other drugs & medical recalls in the United States

  1. 2022-01-19
  2. US
    Drugs & medicalClass II

    Canon Medical System, USA, INC. recalls Flat Panel Detector, Model Number: TFP-800A, used with the Alphenix Systems, Item Numbers: INFX-8000V, INFX-8000C, INFX-8000F,…

    Abnormal images such as horizontal stripes may be displayed and recovery may not not be possible by restarting the system. The worst case scenario is an operator who is working without a workable image may remove a…

    FDA · DeviceCanon Medical System, USA, INC.US Nationwide distribution in the states of DE, FL, LA, MT, NJ, OH, and WV.Official notice →
  3. US
    Drugs & medicalClass II

    Medtronic Perfusion Systems recalls Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM PACK BB10Q85R…

    Product is labeled as non-pyrogenic but endotoxin testing was not performed.

    FDA · DeviceMedtronic Perfusion SystemsWorldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice →
  4. US
    Drugs & medicalClass II

    DePuy Orthopaedics, Inc. recalls GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600

    Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage

    FDA · DeviceDePuy Orthopaedics, Inc.Worldwide distribution - US Nationwide and the countries of Austria,…Official notice →
  5. US
    Drugs & medicalClass II

    PTW NORTH AMERICA CORPORATION recalls Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S080032

    When a measurement with a PTW detector array is performed with the software BeamAdjust 2.2 or VeriSoft 8.0, a measurement error can occur under specific conditions. This error can lead to a too-low or too-high measured…

    FDA · DevicePTW NORTH AMERICA CORPORATIONUS Nationwide distribution in the state of CO.Official notice →
  6. US
    Drugs & medicalClass II

    Haag-Streit USA Inc recalls OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4

    Malfunction of the automatic laser beam shut-off, the OCT unit might not recognize whether the laser beam is safely switched off

    FDA · DeviceHaag-Streit USA IncUS Nationwide distribution in the states of OH, IN.Official notice →
  7. US
    Drugs & medicalClass II

    Philips North America Llc recalls Wireless Footswtich used with the following Philips Allura Xper and Azurion Interventional Fluoroscopic X-ray System . Model Number:…

    Wireless foot switch connection issues causing interruption of Fluoroscopy and exposure

    FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Canada, Australia,…Official notice →
See all drugs & medical recalls →