FDA Device Intelligence
HomeSTRYKER CORPORATION › NA

NA

STRYKER CORPORATION · Model 0295002000 · UDI-DI 04546540892829

LXC Prescription
10
510(k) clearances
20
Adverse events
2
Recalls
12
Facilities

Description

Quick Pressure Monitor Set

Recalls

DateFirmReason
2021-06-28MY01, INC.There is an incorrect version of the needle in the introducer part of devices. The affected Lots were manufactured using needles with a needle trocar geometry which is out of speci
2005-07-22Stryker Instruments Div. of Stryker CorporationThe pressure indicated may be inaccurate, and this inaccuracy may be not detectable by the user.

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.