Drugs & medicalClass II

NOA Medical Industries Inc recalls NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX

Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.

Read the official notice →
Date
2025-01-22
Country
United States
Brand
NOA Medical Industries Inc
Product
NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX
Classification
Class II
Units
US: GA, MI. MA, CA
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-01-22
  2. US
    Drugs & medicalClass II

    Tornier S.A.S. recalls Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during Total Shoulder Arthroplasty.

    The Pin Guide is being recalled because the metal tube may disassemble from the plastic handle. This can result in the Blueprint Mixed Reality headset being unable to detect the Pin Guide and potentially prolonging…

    FDA · DeviceTornier S.A.S.US: MN, KY, MD, MA, TX, AK, TX, ID; France, CanadaOfficial notice →
  3. US
    Drugs & medicalClass II

    Coloplast Manufacturing US, LLC recalls X-Flow prostatectomy catheter, Device Reference Numbers AB6022, AB6024, AB6118, AB6120, AB6122, AB6124, AB6220, AB6222, AB6224,…

    A possible sterility issue was detected in Coloplast's facility on some Coloplast products.

    FDA · DeviceColoplast Manufacturing US, LLCUS Nationwide. Canada.Official notice →
  4. US
    Drugs & medicalClass II

    Augustine Temperature Management, LLC recalls Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) WC77V; 2)…

    HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".

    FDA · DeviceAugustine Temperature Management, LLCWorldwideOfficial notice →
  5. US
    Drugs & medicalClass II

    Karl Storz Endoscopy recalls Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE

    Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance.

    FDA · DeviceKarl Storz EndoscopyUS: AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN,…Official notice →
  6. US
    Drugs & medicalClass II

    Biocartis Nv recalls Idylla INSTRUMENT, IVD, REF P0010. Intended for the detection of nucleic acid targets in various types of human samples, using disposable…

    False-positive MSI-H results generated by the Idylla MSI Test.

    FDA · DeviceBiocartis NvUS: AL, NJ, TX, OH, CAOfficial notice →
  7. US
    Drugs & medicalClass II

    Alcon Research LLC recalls Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description: Monarch¿ III D…

    Increase in complaints associated with a molding defect within the inner lumen of delivery cartridges which could result in a scratch on the intraocular lens (IOL) upon delivery.

    FDA · DeviceAlcon Research LLCUS: AK AL AR AZ CA CO CT DE FL GA GU HI IA ID IL IN KS KY LA MA MD ME MI MN MO…Official notice →
See all drugs & medical recalls →