Recall Atlas
Drugs & medicalClass II

Ferno-Washington Inc recalls Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2…

Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system not operating in powered mode, or exhibiting reduced…

Read the official notice →
Date
2026-10-21
Country
United States
Brand
Ferno-Washington
Product
Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2…
Classification
Class II
Units
Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 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. 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 →
  5. 2022-11-16
  6. 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

    FDA · DeviceFerno-Washington IncNationwide Foreign: BRAZIL BRUNEI CHILE CHINA PERU POLAND PUERTO RICO…Official notice →
All 4 Ferno-Washington recalls →

Other drugs & medical recalls in the United States

  1. 2026-10-21
  2. Drugs & medicalClass II

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    FDA · DeviceBioFire Diagnostics, LLCWorldwide - U.S. Nationwide distribution including in the states and territory…Official notice →
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    INTEGRATED MEDCRAFT LLC recalls FORWARD Gunshot Wound Kit; Model: AFT-GSW;

    Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the sterile pad to degrade over time. The degradation may cause…

    FDA · DeviceINTEGRATED MEDCRAFT LLCUS Nationwide distribution in the states of GA, VA.Official notice →
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    SI-BONE, Inc. recalls iFuse TORQ Implant System Model/Catalog Number: 10055T(10x55mm), 10060T(10x60mm), 10065T(10x65mm), 10080T(10x55mm), 11580T(11.5x80mm)

    The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured.

    FDA · DeviceSI-BONE, Inc.US Nationwide distribution in the states of FL, GA, HI, NC, OH, PA, SD, TX, VA.Official notice →
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    Sarnova HC, Llc recalls Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT

    Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.

    FDA · DeviceSarnova HC, LlcUS Nationwide distribution in the states of IA, IL, IN, KY, MI, MN, MO, ND,…Official notice →
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    Boston Scientific Corporation recalls NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;

    Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this device configuration.

    FDA · DeviceBoston Scientific CorporationUS Nationwide distribution in the states of AL, CA, FL, GA, IL, IN, KY, MD,…Official notice →
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    Neuronetics, Inc. recalls NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number 81-01000-200. Affects the below NeuroStar Advanced…

    Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly.

    FDA · DeviceNeuronetics, Inc.Worldwide distribution - US Nationwide and the countries of Japan and South…Official notice →
See all drugs & medical recalls →