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
Read the official notice →- Date
- 2025-10-22
- Country
- United States
- Brand
- Ferno-Washington
- Product
- FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE IN GROUND TRANSPORTATION AMBULANCES.
- Classification
- Class II
- Units
- US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, IS, IL,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- 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
- 2026-07-29
USFerno-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 →- 2022-11-16
- US
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 →
Other drugs & medical recalls in the United States
- 2025-10-22
- US
Boston Scientific Corporation recalls TENACIO Pump without InhibiZone; UPN: 72404420;
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the country of Canada.Official notice → - US
Medline Industries, LP recalls Medline Adult Anesthesia Set, REF DYNJ39985G
Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.
- US
Iantrek Inc. recalls C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Description: The C-Rex UNO Microinterventional…
Potential for compromised integrity of the sterile packaging.
FDA · DeviceIantrek Inc.US Nationwide distribution in the states of AL, AZ, CA, CT, DE, FL, GA, ID,…Official notice → - US
Insulet Corporation recalls The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field…
The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying feature of the iPhone, while simultaneously selecting a…
- US
Contego Medical LLC recalls Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP System), REF:…
Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter that may not open or may not fully open during sheath retraction and operation of the filter knob. The…
FDA · DeviceContego Medical LLCUS Nationwide distribution in the states of FL, CO, CA, IL, NC, KY, TX, PA,…Official notice → - US
Abbott recalls TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, FJ, (BiD Curve F-J), REF A-TFSE-FJ; cardiac catheter
Abbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.