Recall Atlas
Drugs & medicalClass II

Appliedvr recalls RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.

There is the potential for the program software to malfunction which will not allow it to move forward to the next session.

Read the official notice →
Date
2023-07-05
Country
United States
Brand
Appliedvr
Product
RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.
Classification
Class II
Units
US: NY OUS: None
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2023-07-05
  2. US
    Drugs & medicalClass II

    Exactech, Inc. recalls Exactech Ergo Impactor Handle, Catalog #321-09-05.

    The ball and spring housed within the locking mechanism of the handle can dislodge during disassembly or during impaction.

    FDA · DeviceExactech, Inc.Distribution was made to AR, CA, CO, FL, GA, HI, ID, IL, IN, KS, KY, LA, MD,…Official notice →
  3. US
    Drugs & medicalClass II

    Waldemar Link GmbH & Co. KG (Mfg Site) recalls LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left

    The firm discovered through customer complaints that device segments may not meet specifications.

    FDA · DeviceWaldemar Link GmbH & Co. KG (Mfg Site)Domestic: AL, GA, IL, IN, KS, NJ, NY, and TX. Foreign: Argentina, Australia,…Official notice →
  4. US
    Drugs & medicalClass II

    SEDECAL SA recalls wDR 2.2 Mobile Digital Diagnostic X-Ray System

    There is a software login in issue that may prevent the user from logging in.

    FDA · DeviceSEDECAL SADistribution throughout United States including Puerto Rico and US Virgin…Official notice →
  5. US
    Drugs & medicalClass II

    Beckman Coulter, Inc. recalls Access Hybritech p2PSA reagent, REF B03704 and REF A49752.

    Reagent lot numbers include an insufficient concentration of blocking reagent.

    FDA · DeviceBeckman Coulter, Inc.Distribution was made to CA, CO, CT, FL, GA, IL, IN, MA, MI, NC, NE, NJ, NY,…Official notice →
  6. US
    Drugs & medicalClass II

    Philips North America Llc recalls DigitalDiagnost C90, Model No. 712034 and 712035

    There is a software login in issue that may prevent the user from logging in.

    FDA · DevicePhilips North America LlcDistribution in US: AZ, GA, IN, IA, MN, NE, NH, OH, TX OUS distribution to…Official notice →
  7. US
    Drugs & medicalClass II

    Phadia US Inc recalls Phadia 2500EE instrument -Intended for the in vitro semi-quantitative measurement of IgG antibodies directed to gliadin in human serum or…

    Higher reported results when running EliA GliadinDP IgG Well on the instruments Phadia 2500EE compared to running EliA GliadinDP IgG Well on Phadia 250 instrument

    FDA · DevicePhadia US IncUS: CA, NJ, MIOfficial notice →
See all drugs & medical recalls →