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MID CENTRAL MEDICAL CORP. · Model MCM596 · UDI-DI 10810030862953
10
510(k) clearances
1,818
Adverse events (2 deaths)
37
Recalls
159
Facilities
Description
Stainless Steel Central Sterile Instrument Wrapping Station (Table) with wrapping frame and pull out bins. This stainless steel instrument wrapping station has extra large plastic bins. With the stainless steel top and rack for wrapping instruments in sterile wrap, this table is everything you need. Ergonomic 35 inch work height and heavy duty 4 inch caster that lock in place ensure this table will last for many years. Sturdy work style table design. Removable bins for easy cleaning and reloading instruments. Easy to move but can still look in place with locking casters. .
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-02-14 | Baxter Healthcare Corporation | Three 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 |
| 2017-03-28 | Mizuho OSI | Mizuho 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 |
| 2015-08-17 | Maquet Cardiovascular Us Sales, Llc | Two serious thromboembolic events were reported involving the Adjustable Positioning Elements (Part Number 1007.28A0) in conjunction with Universal Frame (Part Number 1007.24F0) fo |
| 2015-08-17 | Maquet Cardiovascular Us Sales, Llc | Two serious thromboembolic events were reported involving the Adjustable Positioning Elements (Part Number 1007.28A0) in conjunction with Universal Frame (Part Number 1007.24F0) fo |
| 2014-12-19 | Integra LifeSciences Corporation | Through an investigation of complaints, Integra found that there is the possibility for the locking handle mechanism of the Base Units to fail during use. |
| 2014-10-08 | Customed, Inc | Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage condit |
| 2014-10-08 | Customed, Inc | Customed products are being recalled because of compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncont |
| 2014-10-08 | Customed, Inc | Customed products are being recalled because of compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncont |
| 2014-10-08 | Customed, Inc | Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage condit |
| 2014-10-08 | Customed, Inc | Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage condit |
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Get your free API keyRead the docsData 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.