Home › MID CENTRAL MEDICAL CORP. › NA

NA

MID CENTRAL MEDICAL CORP. · Model MCM220-2 · UDI-DI 10810030860591

FOX

510(k) clearances

432

Adverse events (5 deaths)

Recalls

291

Facilities

Description

Chrome IV Pole with Thumb Knob, 2 Hook Top, 5 Leg 22 lb. Base with 3 inch scuff resistant Casters for ease of mobility. 16 inch diameter base space saving base minimizes obstruction in the operating room where floor space is essential. Base is also weighted to make it more stable and lower the center of gravity. Base available in 5 different colors which is ideal for asset retention in a department and for departmentalization. Rubber bumpers on end of base legs to help protect walls and other objects from scuffing. 1 inch diameter chrome pole adjusts 50 inches to 92 inches with friction lock knob. 2 hook rams horn style top ensures bags are held securely yet easy to remove and put on. A great IV Pole for anywhere space is at a premium.

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 key Read 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.