FDA Device Intelligence
Home › MID CENTRAL MEDICAL CORP. › NA

NA

MID CENTRAL MEDICAL CORP. · Model MCM740 · UDI-DI 10810030863011

FWZ
10
510(k) clearances
1,831
Adverse events (2 deaths)
37
Recalls
159
Facilities

Description

Mayo Tray Attachment. This Mayo Tray attaches directly to the OR Table rail for convenience and to save space in the OR. The 5/8" mounting post attaches easily to the table rail with a standard Clark Socket (sold separately). Stainless Steel construction for longevity and ease of cleaning. Height adjustable up to 26". Tray removes for easy cleaning. .

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, 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
2014-10-08Customed, IncSignificant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage condit

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.