Drugs & medicalClass II

Ferno-Washington Inc recalls FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V Li-Ion Batteries Model Number #0822484/0822483 Note: Transcend…

Batteries could become unstable when not properly maintained and/or subjected to repeated drops, power washing directly into battery contacts or abuse, may result in a fire and/or injury

Read the official notice →
Date
2022-11-16
Country
United States
Brand
Ferno-Washington
Product
FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V Li-Ion Batteries Model Number #0822484/0822483 Note: Transcend…
Classification
Class II
Units
Nationwide Foreign: BRAZIL BRUNEI CHILE CHINA PERU POLAND PUERTO RICO…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Ferno-Washington recalls

  1. 2026-07-29
  2. US
    Drugs & medicalClass II

    Ferno-Washington Inc recalls Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only. Designed to load,…

    Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case condition, rail mechanism may become lodged during operation and…

    FDA · DeviceFerno-Washington IncWorldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, GA,…Official notice →
  3. 2025-10-22
  4. US
    Drugs & medicalClass II

    Ferno-Washington Inc recalls FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE IN GROUND TRANSPORTATION AMBULANCES.

    The fastening post hardware could loosen allowing the fastening post to detach from the cot

    FDA · DeviceFerno-Washington IncUS Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, IS, IL,…Official notice →
All 3 Ferno-Washington recalls →

Other drugs & medical recalls in the United States

  1. 2022-11-16
  2. US
    Drugs & medicalClass II

    Avanos Medical, Inc. recalls Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as: SUMMIT MEDICAL…

    Sterile extension sets were distributed without an expiration date

    FDA · DeviceAvanos Medical, Inc.US: CA, CO, FL, MI, NM, OH, OR, TN, TX, UT, WIOfficial notice →
  3. US
    Drugs & medicalClass II

    Medtronic MiniMed recalls Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711, MMT-1712, MMT-1751, MMT-1752

    Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series Insulin Pump Systems associated with the communication protocol that could allow unauthorized access to the pump system. This unauthorized…

    FDA · DeviceMedtronic MiniMedUS: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS,…Official notice →
  4. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Cardinal Health GEL PACK REUSABLE, SMALL, Cat. 70204

    Users are being informed that the product should not be used on infants/neonates. A caution statement will be added to the labeling stating: Not for use on Infants/Neonates .

    FDA · DeviceCardinal Health 200, LLCnationwide and CanadaOfficial notice →
  5. US
    Drugs & medicalClass II

    iRhythm Technologies, Inc. recalls Zio AT Clinical Reference Manual, Part: ALB0031, and Zio AT Important Information Pamphlet, Part: ALB0034. For Zio Ambulatory ECG…

    Ambulatory ECG monitoring system labeling update: 1) Clinically actionable arrhythmia notifications delayed until patient registration is complete; 2) Patches limited to 100 symptomatic and 500 asymptomatic wireless…

    FDA · DeviceiRhythm Technologies, Inc.US: MD, NY, FL, TN, WA, AL, MA, AZ, CA, KS, HI, PA, NJ, TX, MN, VA, AR, OR,…Official notice →
  6. US
    Drugs & medicalClass II

    SEDECAL SA recalls Sedecal Soltus Battery Mobile X-Ray System REF Soltus 450 Battery Mobile X-Ray System REF Soltus 500

    Due to un-commanded movement of mobile x-ray unit.

    FDA · DeviceSEDECAL SAU.S.: KY, WI, FL, DE, WV, CA, MO, NY, NC, AL, AR, MS, GA, IL, IA, TN, KS, KY,…Official notice →
  7. US
    Drugs & medicalClass II

    Fresenius Medical Care Holdings, Inc. recalls NaturaLyte Liquid Acid concentrate, Part Number 08-0231-4, four (4) one-gallon bottles per bottle case. For dialysis.

    The "Nominal Chemical Composition" section of the label incorrectly lists 5.62g/L KCL (potassium chloride). 5.62g/L actually corresponds to the CaCl (calcium chloride) content. The product remains potassium free.

    FDA · DeviceFresenius Medical Care Holdings, Inc.Domestic distribution to AL AZ CA DC FL GA HI IL IN MD MI MO MS NE NJ NY OH PA…Official notice →
See all drugs & medical recalls →