Home › L I N E T spol. s r.o. › Sprint 100
Sprint 100
L I N E T spol. s r.o. · Model 1ES15302-2 · UDI-DI 08592654150573
10
510(k) clearances
35,224
Adverse events (108 deaths)
76
Recalls
109
Facilities
Description
The Sprint Stretcher transport bed in its basic option used for transport and for X-ray scanning is designed for the transport of critical patients being admitted in emergency conditions.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-06-19 | Ferno-Washington Inc | 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 b |
| 2025-09-11 | Ferno-Washington Inc | The fastening post hardware could loosen allowing the fastening post to detach from the cot |
| 2023-05-24 | Stryker Medical Division of Stryker Corporation | Base leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lowering the cot, cot tip |
| 2023-02-01 | Stryker Medical Division of Stryker Corporation | Transport 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 foot end from the cot |
| 2023-01-18 | Linet 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. |
| 2022-11-11 | Stryker Medical Division of Stryker Corporation | Cot 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 lowering faster than |
| 2022-10-07 | Ferno-Washington Inc | 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 |
| 2021-05-12 | Stryker Medical Division of Stryker Corporation | Medical 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 labeling accurately iden |
| 2021-05-12 | Stryker Medical Division of Stryker Corporation | Medical 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 labeling accurately iden |
| 2021-05-12 | Stryker Medical Division of Stryker Corporation | Medical 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 labeling accurately iden |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.