FDA Device Intelligence
HomeDevice types › FPO

Stretcher, Wheeled

FDA product code FPO · Class 2 · General Hospital

677
Registered devices
35,224
Adverse events
76
Recalls
50
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-06-19Ferno-Washington IncProduct may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case condition,
2025-09-11Ferno-Washington IncThe fastening post hardware could loosen allowing the fastening post to detach from the cot
2023-05-24Stryker Medical Division of Stryker CorporationBase leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lower
2023-02-01Stryker Medical Division of Stryker CorporationTransport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or fo
2023-01-18Linet Spol. S.r.o.Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.
2022-11-11Stryker Medical Division of Stryker CorporationCot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot l
2022-10-07Ferno-Washington IncBatteries could become unstable when not properly maintained and/or subjected to repeated drops, power washing directly into battery contacts or abuse, may resu
2021-05-12Stryker Medical Division of Stryker CorporationMedical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labe
2021-05-12Stryker Medical Division of Stryker CorporationMedical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labe
2021-05-12Stryker Medical Division of Stryker CorporationMedical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labe

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.