FDAJuly 27, 2023device

Guider Softip Guide Catheter 5F 90CM MULTI PURPOSE, Catalog number M003100630, cardiac guide catheter

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

The hazard

Stryker Neurovascular has observed that certain lots of Guider Softip XF Guide Catheters appear to have the incorrect tip curve shape. The impacted products were distributed with a tip curve shape which differs from the labeled tip curve shape.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

08714729283515

Recall history

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

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Guider Softip Guide Catheter 5F 90CM MULTI PURPOSE, Catalog number M003100630, cardiac guide catheter — Recall Details · AllClear