Drugs & medicalClass II

Agfa N.V. recalls DR 800. Digital Radiography X-ray System.

Potential for the front lever chain of the DR 800 table to fail.

Read the official notice →
Date
2024-09-04
Country
United States
Brand
Agfa N.V
Product
DR 800. Digital Radiography X-ray System.
Classification
Class II
Units
Worldwide - US Nationwide distribution in the states of CA, FL, IL, IN, KS,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Agfa N.V recalls

  1. 2024-04-10
  2. US
    Drugs & medicalClass II

    Agfa N.V. recalls Agfa DX-D 100 system-Digital Radiography mobile X-ray System. A mobile X-Ray modality, consisting of X-Ray console, generator, tube,…

    Steel cable installed inside the mobile column which supports the weight of the telescopic arm with the tube head has potential risk -an interference could cause the safety system which blocks the arm if the cable is…

    FDA · DeviceAgfa N.V.Worldwide distribution - US Nationwide and the countries of Canada, Argentina,…Official notice →
All 2 Agfa N.V recalls →

Other drugs & medical recalls in the United States

  1. 2024-09-04
  2. US
    Drugs & medicalClass II

    Beaver Visitec International, Inc. recalls BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001113;

    Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in some of BVI CustomEyes Procedure…

    FDA · DeviceBeaver Visitec International, Inc.US Nationwide distribution.Official notice →
  3. US
  4. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedural kits labeled as: ARTHROGRAPH TRAY, Pack Number MNS12670A

    Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwideOfficial notice →
  5. US
    Drugs & medicalClass II

    RONAN MEDICAL LLC recalls BrainFeedback Pro 2 Device - is intended as an instrument that provides a visual and auditory signal corresponding to the status of a…

    Neurofeedback systems removed due to missing design and development documentation and devices may not perform as intended.

    FDA · DeviceRONAN MEDICAL LLCWorldwide - US Nationwide distribution in the states of CA, FL, TN, MI, IL, CT…Official notice →
  6. US
    Drugs & medicalClass II

    Abbott Diagnostics Technologies AS recalls Afinion 2 Analyzer, model #1116986, US refurbished, CLIA waived.

    Five Afinion 2 (AF2) Analyzer were incorrectly market configured as Moderate Complexity and distributed to customers. Use of moderately complex assays by waived laboratories could result in erroneous results.

    FDA · DeviceAbbott Diagnostics Technologies ASUS Nationwide distribution in the states of AZ, IN, MA, MN, and OH.Official notice →
  7. US
    Drugs & medicalClass II

    Beckman Coulter, Inc. recalls DxI 9000 Access Immunoassay Analyzer, Catalog #C11137.

    When a DxI 9000 Access Immunoassay Analyzer is connected to a Laboratory Automation System (LAS) and is running with the system software versions 1.17.0 and below, the analyzer does not send a message to the LAS when…

    FDA · DeviceBeckman Coulter, Inc.Worldwide - US Nationwide distribution in the states of CA, FL, GA, IN, KS,…Official notice →
See all drugs & medical recalls →