Recall Atlas
Drugs & medicalClass I

Emergent Protective Products USA Inc recalls RSDL (Reactive Skin Decontamination Lotion) Kit, NSN 6505-21-912-5229. Used to remove and/or neutralize chemical warfare…

Complaints of leaking packets were received.

Read the official notice →
Date
2023-01-18
Country
United States
Brand
Emergent Protective Products USA Inc
Product
RSDL (Reactive Skin Decontamination Lotion) Kit, NSN 6505-21-912-5229. Used to remove and/or neutralize chemical warfare agents and T-2…
Classification
Class I
Units
Distribution to US state of VA (distributor), Canada, and Switzerland
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2023-01-18
  2. US
    Drugs & medicalClass II

    Ventana Medical Systems, Inc. recalls VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD Predictive)…

    Internal comparison studies revealed unacceptable, light staining. Light staining affects the borderline of positive versus negative test results. It can cause a reduction in both staining intensity and the percent…

    FDA · DeviceVentana Medical Systems, Inc.Worldwide distribution - U.S. Nationwide distribution including in the states…Official notice →
  3. US
    Drugs & medicalClass I

    Philips Respironics, Inc. recalls Philips Trilogy 100 Ventilator, Model Numbers 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT1054260, 1054096B,…

    The replacement silicone sound abatement foam installed into some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing to which it is attached. If this were to happen, the foam could potentially…

    FDA · DevicePhilips Respironics, Inc.US Nationwide and Global Distribution to countries of: Australia, Brazil,…Official notice →
  4. US
    Drugs & medicalClass I

    Covidien LP recalls MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter, Sterile, Single Use, Rx Only: 13.5cm, Straight Extensions, Kit - Model No.…

    There is a potential leaking condition within the hub of affected devices, due to an inter-lumen void in the hub component, which may result in unanticipated fluid return during use.

    FDA · DeviceCovidien LPWorldwide distribution. US nationwide including Guam, USVI, and Puerto Rico;…Official notice →
  5. US
    Drugs & medicalClass II

    Northern VA Compounders PLLC recalls QuadMix Plus (PGE1/Papaverine HCl/Phentolamine Mesylate/Atropine) 20mcg/30mg/2mg/0.2mg/mL INJECTABLE, packaged in 2.5 mL…

    Lack of Assurance of Sterility

    FDA · DrugNorthern VA Compounders PLLCNationwide in the USAOfficial notice →
  6. US
    Drugs & medicalClass II

    Direct Rx recalls Moxifloxacin Ophthalmic Solution, 0.5%, 3 mL, Rx Only, Packaged and Distributed By: Direct Rx, LLC 94 Worldwide Drive, Dawsonville, GA…

    cGMP deviation: discontinue of stability support for product.

    FDA · DrugDirect RxFLOfficial notice →
  7. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Rifampin Capsules USP, 300 mg, 30-count bottle; Rx Only, Manufactured for: Lupin Pharmaceuticals Baltimore, Maryland 21202,…

    Failed Impurities/Degradation Specifications: Failure observed in related substance testing during long term stability study.

    FDA · DrugLupin Pharmaceuticals Inc.Distributed Nationwide in the USAOfficial notice →
See all drugs & medical recalls →