Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only. Desi

FDA device recall Z-2760-2026 · posted 2026-07-17 · Open, Classified

Recall details

Recalling firm

Ferno-Washington Inc

Reason for recall

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 movement of the stretcher along the rail may no longer be possible through either powered or manual operation. May cause delays in transport of patient to healthcare facility.

Action taken

On June 19. 2026, the firm began notifying customers via Urgent Medical Device Correction letters. Customers were instructed to contact Ferno for assistance if abnormal rail movement, increased resistance during rail extension or retraction, or other unusual rail operation is observed. Ferno will contact all affected customers directly and dispatch trained field service personnel to perform the correction onsite at customer locations. The correction does not require removal of the PF2 Fastening System from service prior to the scheduled repair. The field correction consists of replacement of the affected roller assembly with an updated assembly manufactured in accordance with revised assembly requirements intended to eliminate the potential for interference and subsequent roller deformation.

Root cause

Process control

Status

Open, Classified

Product code

FPO

Quantity affected

278

Distribution

Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, GA, IA, ID, IL, IN, KY, LA, MD, ME, MN, MO, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV and the count

Date initiated

2026-06-19

Date posted

2026-07-17

Location

Wilmington, OH