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Recall Observatory FDA recall evidence

Device product

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.

Z-1912-2026

March 11, 2026

Class II

Product summary

Firm
ARROW INTERNATIONAL, LLC
Event
Event 98618
Status
Ongoing
Classification
Class II
Quantity
115
Official record key
device-enforcement:Z-1912-2026

Official wording

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

Code information: Product code:ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 Batch Number: 33F25K0130

Distribution pattern: U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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