FDA Device Intelligence
HomeMID CENTRAL MEDICAL CORP. › NA

NA

MID CENTRAL MEDICAL CORP. · Model MCM760 · UDI-DI 10810030863097

FWZ
10
510(k) clearances
1,818
Adverse events (2 deaths)
37
Recalls
159
Facilities

Description

SS Thumb controlled Mayo Stand. Removable Tray for easy cleaning. Designed so a surgeon or nurse can adjust the height of the stand while sterile and while seated without compromising the drape. Single post design makes it easy to maneuver into position right where you want it. Solid stainless steel construction. Brass inserts for smoother adjustment. 2" double ball bearing premium rubber casters. Thumb operated lock adjusts height from 36"-62". Low profile base design easily slides under O.R. table. .

Recalls

DateFirmReason
2024-02-14Baxter Healthcare CorporationThree lots of the Boot Assembly, Traction Device are being recalled due to due to a customer report of an incorrectly oriented locking pin which caused the boot to detach from the
2017-03-28Mizuho OSIMizuho has discovered that the 5319-37 Wilson Frame Pads have a design deficiency in the construction of their mounting sleeves that may allow the patient to contact the underlying
2015-08-17Maquet Cardiovascular Us Sales, LlcTwo serious thromboembolic events were reported involving the Adjustable Positioning Elements (Part Number 1007.28A0) in conjunction with Universal Frame (Part Number 1007.24F0) fo
2015-08-17Maquet Cardiovascular Us Sales, LlcTwo serious thromboembolic events were reported involving the Adjustable Positioning Elements (Part Number 1007.28A0) in conjunction with Universal Frame (Part Number 1007.24F0) fo
2014-12-19Integra LifeSciences CorporationThrough an investigation of complaints, Integra found that there is the possibility for the locking handle mechanism of the Base Units to fail during use.
2014-10-08Customed, IncSignificant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage condit
2014-10-08Customed, IncCustomed products are being recalled because of compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncont
2014-10-08Customed, IncSignificant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage condit
2014-10-08Customed, IncSignificant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage condit
2014-10-08Customed, IncCustomed products are being recalled because of compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncont

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.