Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Ferno-Washington with 10 device recalls and 5 510(k) clearances. The most recent is a device recall dated Jun 19, 2026: Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intend….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 19, 2026 | Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only. Designed to load, unloClass II · Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly | Device recalls |
| Apr 28, 2026 | Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2 Premium,Class II · Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stret | Device recalls |
| Sep 11, 2025 | FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE IN GROUND TRANSPORTATION AMBULANCES.Class II · The fastening post hardware could loosen allowing the fastening post to detach from the cot | Device recalls |
| Oct 7, 2022 | FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V Li-Ion Batteries Model Number #0822484/0822483 Note: TransceClass II · Batteries could become unstable when not properly maintained and/or subjected to repeated drops, power washing directly | Device recalls |
| Mar 8, 2017 | Ferno PROFlexx¿ Model 28Z Chair CotClass II · The recall was initiated as a result of the detection of an incorrect nut used in manufacturing. | Device recalls |
| Mar 10, 2016 | Poly-bags containing splint strap labeled with "Pediatric" sticker. Each strap kit contains adjustable length leg straps, ankle wrap, a tClass II · On March 9, 2016, the firm was contacted regarding the possibility of incorrect labeling on the outside poly- bag of the | Device recalls |
| Mar 10, 2016 | Poly-bags containing the strap labeled with "Adult" sticker. Each strap kit contains adjustable length leg straps, ankle wrap, a thigh paClass II · On March 9, 2016, the firm was contacted regarding the possibility of incorrect labeling on the outside poly- bag of the | Device recalls |
| Aug 3, 2015 | Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital patient transport.Class II · Hole elongation in the telescoping load frame channel. A hole elongation could affect the ability of the retention pin t | Device recalls |
| Apr 21, 1998 | FERNO HEALTHCARE RECLINE-A-BATH 2K980033 · ILJ | 510(k) clearances |
| Sep 9, 1993 | FERNO WASHINGTON INCUBATOR TRANSPORTER, MOD. 35-ITK932417 · FPL | 510(k) clearances |
| Dec 17, 1986 | MODEL 668, TRACTION SPLINT, ADULTK864765 · HST | 510(k) clearances |
| Nov 13, 1986 | MODEL 35-B ALL LEVEL COTK864269 · FPO | 510(k) clearances |
| Sep 12, 1986 | EZ LOAD MODEL 30, ALL LEVEL COTK862441 · FPO | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
