FDAMarch 11, 2026device

PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 The Arrow¿ percutaneous sheath introducer permits venous access and catheter introduction to the central circulation.

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

The hazard

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

What to do

FDA enforcement status: Ongoing

Brands named

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UPCs

10801902159127

Recall history

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

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PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 The Arrow¿ percutaneous sheath introducer permits venous access and catheter introduction to the central circulation. — Recall Details · AllClear