FDA Device Intelligence
HomePEDICRAFT, INC. › Pedicraft

Pedicraft

PEDICRAFT, INC. · Model 18215 · UDI-DI 00766923182154

NZG Prescription
0
510(k) clearances
104
Adverse events
2
Recalls
25
Facilities

Description

u-design bassinet drawer/shelf

Recalls

DateFirmReason
2018-10-10Stryker Medical Division of Stryker CorporationIt was identified that the volume of air inside the mattress may expand in regions of high altitude which may result in an unintended gap between the plateau of the inflated patien
2011-10-14Nemschoff Chairs, Inc.To correct issues with casters, door hinges, drawer slides, and the bassinet surround. Also, to add labeling to the product regarding specific instructions for cleaning the bassin

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 docs
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.