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FDAJune 2, 2016device

ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER. Product Usage: Indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring cental venous access including, but not limited to: multiple infusions of fluid...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Arrow is recalling these products due to the possibility that although the kit is labeled as containing a 20 cm catheter, a 16 cm catheter may be packaged in the kit.

What to do

FDA enforcement status: Terminated

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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