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MID CENTRAL MEDICAL CORP. · Model MCM286 · UDI-DI 10810030860997

FOX

510(k) clearances

433

Adverse events (5 deaths)

Recalls

290

Facilities

Description

SS Double IV Pole W/Thumb Knob, 4 Hook Top, 6 Leg Spider Base, 3 inch casters, steering wheel and Tray. This IV Pole is designed for areas where several infusion pumps are needed such as ICU. 6 leg base is 22 inch diameter and has a low center of gravity with enhanced weight for added stability.Standard epoxy coated base color is charcoal. Colored bases (Red, Blue, Yellow, Green) are available at no extra charge to help each department maintain their assets. 3 inch scuff resistant casters are standard for ease of mobility. Double poles make more spots to hang pumps and the two four hook tops make it easier to keep IV lines organized. Height adjusts from 85 inch to 110 inch. Full circle steering wheel makes it easy to maneuver from any side. Complete pole construction is 304 grade stainless steel. Removable plastic tray makes a great place for storage and a spot to set things during bag changes and setup.

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

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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.