Home › MID CENTRAL MEDICAL CORP. › NA
NA
MID CENTRAL MEDICAL CORP. · Model MCM252 · UDI-DI 10810030860799
10
510(k) clearances
432
Adverse events (5 deaths)
5
Recalls
291
Facilities
Description
8 Hook SS Lift Assist IV Pole. Helps eliminates Back Injuries. Easily lifts heavy loads by simply turning the crank. Height adjustable from 56 inch 96 inch high. Six Leg epoxy coated steel tube base offers the stability you need. 3 inch scuff resistant casters provide unmatched maneuverability. Base post is 2 inch square stainless steel tube. 8 hook rams horn style top.Extension post is one and one quarter stainless steel tube. No electric motors or hydraulic pumps to replace. A great fit for cases that require large volumes of fluid for irrigation.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-12-01 | Ohmeda Medical | There is the potential for the Rotating IV Pole to fall. A fall could result in an injury to a bystander holding the patient or to the operator. |
| 2017-08-24 | Firefly Medical, Inc. | The dowel pins (P/N 16082) that fit in the left and right leg pivot castings (P/Ns 16049/16056) can rotate and gradually maneuver out of the leg casting after several hundred deplo |
| 2016-11-01 | Firefly Medical, Inc. | The dowel pin could potentially slip out of its press fit, resulting in the product potentially slumping to one side which could cause the patient to stumble. |
| 2016-08-22 | EKOS Corporation | Casters on the EKOS carts may be missing washers which can cause premature wear and dislodgement of the casters/wheels leading to failure. |
| 2015-10-13 | Stryker Medical Division of Stryker Corporation | It was identified by a customer complaint that some I.V. poles were retracting/lowering from an extended position to the low height unexpectedly. An investigation was initiated whi |
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 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.
