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MID CENTRAL MEDICAL CORP. · Model MCM344 · UDI-DI 10810030861352
10
510(k) clearances
42
Adverse events (1 deaths)
9
Recalls
115
Facilities
Description
18 inch L Horizontal Traction Tower for Rectangular Tables. Solid Stainless Steel Construction. Adapts easily to most arm and hand tables. For Mid Central Medical Tables, It simply attaches to blue clamp that hold the leg. .75 inch outside square tube with .5 inch telescoping tube provides the strongest and most dependable device available. Knob tightens at any position. Comes with cable and connections for traction devices.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-12-14 | Smith & Nephew, Inc. | Products were shipped to the Global Distribution Center instead of the sterilizer and therefore product did not undergo the sterilization process |
| 2018-06-21 | Ossur Americas | Halo system products labeled MR conditional will undergo confirmatory safety testing to confirm MR conditional parameters. In addition, the second line description on the titanium |
| 2018-06-21 | Ossur Americas | Halo system products labeled MR conditional will undergo confirmatory safety testing to confirm MR conditional parameters. In addition, the second line description on the titanium |
| 2016-03-14 | Ossur H / F | There is a potential for partial or complete fracture of the plastic stabilizer strap on the vest. |
| 2016-03-14 | Ossur H / F | There is a potential for partial or complete fracture of the plastic stabilizer strap on the vest. |
| 2016-03-14 | Ossur H / F | There is a potential for partial or complete fracture of the plastic stabilizer strap on the vest. |
| 2016-03-14 | Ossur H / F | There is a potential for partial or complete fracture of the plastic stabilizer strap on the vest. |
| 2016-03-14 | Ossur H / F | There is a potential for partial or complete fracture of the plastic stabilizer strap on the vest. |
| 2016-03-14 | Ossur H / F | There is a potential for partial or complete fracture of the plastic stabilizer strap on the vest. |
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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.