Ferno-Washington Inc

Complete recall history across all FDA and CPSC categories — 8 total recalls

Ferno-Washington Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (8)

FDA medical device enforcement actions by Ferno-Washington Inc

Date Product Reason Class
Sep 11, 2025 FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE ... The fastening post hardware could loosen allowing the fastening post to detac... Class II
Oct 7, 2022 FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V ... Batteries could become unstable when not properly maintained and/or subjected... Class II
Mar 8, 2017 Ferno PROFlexx¿ Model 28Z Chair Cot The recall was initiated as a result of the detection of an incorrect nut use... Class II
Mar 10, 2016 Poly-bags containing the strap labeled with "Adult" sticker. Each strap ki... On March 9, 2016, the firm was contacted regarding the possibility of incorre... Class II
Mar 10, 2016 Poly-bags containing splint strap labeled with "Pediatric" sticker. Each s... On March 9, 2016, the firm was contacted regarding the possibility of incorre... Class II
Aug 3, 2015 Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System ... Hole elongation in the telescoping load frame channel. A hole elongation coul... Class II
May 1, 2015 Wheel caster set screw for Ferno iNX Wheeled Stretcher. Ferno iNX Wheeled St... The firm discovered an improperly installed set screw in one caster arm assem... Class II
Dec 3, 2014 Ferno Model 35X PROFlexx Stretchers, one unit per package The wheel castor assemblies may be loosening on the stretchers. Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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