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…
Read the official notice →- Date
- 2026-07-29
- Country
- United States
- Brand
- Ferno-Washington
- Product
- Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only. Designed to load,…
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, GA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2025-10-22
USFerno-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 →- 2022-11-16
- US
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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
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Other drugs & medical recalls in the United States
- 2026-07-29
- US
AVID Medical, Inc. recalls Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the state of California.Official notice → - US
SEASPINE ORTHOPEDICS CORPORATION recalls SeaSpine Polyaxial Head REF Number: 41-3010
Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
FDA · DeviceSEASPINE ORTHOPEDICS CORPORATIONWorldwide - US Nationwide distribution including in the states of Alabama,…Official notice → - US
Olympus Corporation of the Americas recalls Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying…
Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.
FDA · DeviceOlympus Corporation of the AmericasWorldwide - US Nationwide distribution in the states of OH, CA, NJ, FL and the…Official notice → - US
ICU Medical Inc. recalls Hotline Fluid Warming Set, single use device, is designed to warm blood and intravenous fluids and deliver them to the patient's…
ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent application at the tubing to return connector bond.
- US
Paragon 28, Inc. recalls P28 PHANTON INTRAMEDULLARY NAIL SYSTEM, Phantom Hindfoot TTC/TC Ball Tipped Guide Rod, SIZE: 0.30 mm, LENGTH: 800 mmm, ITem number…
Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging.
FDA · DeviceParagon 28, Inc.US nationwide, Australia, Canada, The Netherlands, and New ZealandOfficial notice → - US
Boston Scientific Corporation recalls FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number…
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orientation during device preparation. Valve…