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Drive Devilbiss Healthcare · Model P903SC05 · UDI-DI 00822383000442

OSI Prescription
0
510(k) clearances
1,441
Adverse events (13 deaths)
4
Recalls
31
Facilities

Description

Product Description P903 Staff control for Ti-Motion Motors

Recalls

DateFirmReason
2025-10-31Stryker Medical Division of Stryker CorporationStryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential inten
2014-03-18SCM True Air Technologies LLCThe firm is recalling the products due to lack of design controls, lack of a Device Master Record, and failure to approve specific vendors.
2014-03-18SCM True Air Technologies LLCThe firm is recalling the products due to lack of design controls, lack of a Device Master Record, and failure to approve specific vendors.
2012-08-02Kreg Medical Inc.An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during patient use, leaving the patient in a forward tilt position.

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Data 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.