Drugs & medicalClass II

DeRoyal Industries Inc recalls DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)

Sterile wound dressing, lacks sterility assurance

Read the official notice →
Date
2026-06-10
Country
United States
Brand
DeRoyal Industries
Product
DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)
Classification
Class II
Units
US Nationwide distribution in the states of FL & NC.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 DeRoyal Industries recalls

  1. 2026-09-30
  2. US
    Drugs & medicalClass II

    DeRoyal Industries Inc recalls REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series

    Myocardial temperature probes contain an incorrect needle. Specifically, an 18mm needle was included instead of a 15mm needle.

    FDA · DeviceDeRoyal Industries IncUS Nationwide distribution in the states of LA,MO, MD, TN, UT.Official notice →
  3. 2025-03-12
  4. US
    Drugs & medicalClass II

    DeRoyal Industries Inc recalls DeRoyal REF 71-C5100NS Tubing, Suction, Connector; DeRoyal REF 71-C6100NS Tubing, Suction, Connector; DeRoyal REF 71-C7100NS Tubing,…

    Due to the inner diameter of the suction tubing connector being smaller than the suction canister lid port connection. This size difference, combined with the durometer of the plastic material, makes the assembly to a…

    FDA · DeviceDeRoyal Industries IncU.S.: IL, MN, NC, PA, and VA O.U.S.: N/AOfficial notice →
  5. 2025-02-26
  6. US
    Drugs & medicalClass II

    DeRoyal Industries Inc recalls DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid movement

    The tubing may not ensure that the yankauer stays intact, and secure to the tubing / yankauer connection for a tight seal. This could result in inadequate suction and cause delay in patient care.

    FDA · DeviceDeRoyal Industries IncU.S.: ND, NY, VA, WV, NJ, TN, OK, TN, GA, OH, MN, AZ, WI, IL, MA, MD, MO, AR,…Official notice →
  7. 2024-11-13
  8. US
    Drugs & medicalClass II

    DeRoyal Industries Inc recalls DeRoyal CHILDREN'S LAPTRACEPACK, 89-9362.06

    DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual…

    FDA · DeviceDeRoyal Industries IncUS Nationwide distribution in the state of OH.Official notice →
  9. 2024-04-03
  10. US
    Drugs & medicalClass I

    DeRoyal Industries Inc recalls GeoMed Custom Tracecarts, REF Numbers: a) 53-1831 ORTHO TOTAL JOINT TRACECART, b) 53-1836 GENERAL SURGERY TRACECART

    DeRoyal manufactured and distributed Surgical Tracecarts that contain a Nurse Assist 16FR Silver Urine Meter Foley which were subsequently recalled.

    FDA · DeviceDeRoyal Industries IncFloridaOfficial notice →
  11. 2024-01-03
  12. US
    Drugs & medicalClass II

    DeRoyal Industries Inc recalls DeRoyal CARDIAC CATH SET-UP KIT PGYBK, REF 89-10572

    Kit were manufactured and distributed with Edwards Life Sciences TruWave Disposable pressure transducers which were subsequently recalled by Edwards Life Sciences.

    FDA · DeviceDeRoyal Industries IncUS: VirginiaOfficial notice →
All 18 DeRoyal Industries recalls →

Other drugs & medical recalls in the United States

  1. 2026-06-10
  2. US
    Drugs & medicalClass II

    Grace Medical, Inc. recalls TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis

    Due to incorrect functional length on device labeling.

    FDA · DeviceGrace Medical, Inc.U.S Nationwide distribution in the state of MD.Official notice →
  3. US
    Drugs & medicalClass II

    Windstone Medical Packaging, Inc. recalls Aligned Medical AMS16835 Fluids Kit RX

    Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.

    FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of IL, VA.Official notice →
  4. US
    Drugs & medicalClass II

    GE Medical Systems China Co., Ltd. recalls MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph

    Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. This could impact clinical…

    FDA · DeviceGE Medical Systems China Co., Ltd.Worldwide - US Nationwide distribution in the states of Florida and Georgia.…Official notice →
  5. US
    Drugs & medicalClass II

    CareFusion 303, Inc. recalls BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet

    Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

    FDA · DeviceCareFusion 303, Inc.US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ,…Official notice →
  6. US
    Drugs & medicalClass II

    Bayer Medical Care, Inc. recalls Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog…

    Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock cannot be reliably engaged with the…

    FDA · DeviceBayer Medical Care, Inc.Worldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice →
  7. US
    Drugs & medicalClass II

    Daavlin Distributing Company recalls Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis,…

    Some of the Calibration/Output Certificates had the outputs reversed.

    FDA · DeviceDaavlin Distributing CompanyUS Nationwide distribution.Official notice →
See all drugs & medical recalls →