Multi-Med, Inc.: Marquette Medical Huber Trap-A Safety Huber Needle 20ga x .75" Winged Administration Set w/Y Site Model # MWS203 Intended to be used to inject fluids into, withdraw fluids from inside the vascular space through a subcutaneously implanted port.

Recall number

Z-2558-2010

Recalling firm

Multi-Med, Inc.

Product

Marquette Medical Huber Trap-A Safety Huber Needle 20ga x .75" Winged Administration Set w/Y Site Model # MWS203 Intended to be used to inject fluids into, withdraw fluids from inside the vascular space through a subcutaneously implanted port.

Status

Terminated

Initiated

2010-08-30

Posted

2010-09-29

Terminated

2013-01-31

Reason

Huber needles may core and result in port leakage or emboli being flushed our of the port.

Root cause

Device Design

Action

Multi-Med issued an Urgent: Medical Device Recall notification on 8/30/10 via fax and followed by hard copy letter. Users were advised of the problem and asked to immediately examine their inventory and quarantine the affected product. They were to also notify their customers of the recall. The firm stated in the letter that they would contact customers to determine the number of product that they had and the amount they expected from the field. The firm will coordinate a plan for the return of the affected product. Questions should be directed to Sue Starkey at 603-357-8733.

Quantity

31,350 units

Distribution

Worldwide Distribution -- USA and Mexico.

Lot, serial or model codes

Lot Code: 5G020M 5G039M 5I031M 6A052M 6B029M 6F048M 6J012M 6L014M 7B021M 7C068M 7H062M 7K051M 7L022M 8B053M 8G009M 8L019M 9A012M 9C033M 9K048M 0B053M 0C050M

510(k) numbers

["K891919"]

PMA numbers

not on file

Product code

FMI

Firm FEI

1221765

Firm city

Keene

Firm state

NH

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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