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Recall Observatory FDA recall evidence

Device product

Arrowgard Blue and Arrowgard Blue Plus Pressure Injectable Central Venous Catheter, a multiple-lumen catheter that permits venous access to central circulation. Catalog number ASK-45703-PHF.

Z-1633-2014

July 17, 2013

Class II

Product summary

Firm
Arrow International Inc
Event
Event 67833
Status
Terminated
Classification
Class II
Quantity
4285
Official record key
device-enforcement:Z-1633-2014

Official wording

Reason: The labeling states that the kit contains Introducer Needle: Echogenic 18 Ga. x 2.5 (6.35cm) XTW and 5mL ArroW Raulerson Spring-Wire Introduction Syringe; however, the kit contains, and should state, Introducer Needle: 18 Ga. x 2.5 (6.35cm) XTW and 5mL ArroW Raulerson Spring-Wire Introduction Syringe. As a result of this labeling inconsistency, if the clinician were to place the needle under x-r

Code information: MF2016829 RM2072044 RM2034076 RM2095792 RM2056629 RM3015571 RM2069733

Distribution pattern: US Distribution only to MI.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The labeling states that the kit contains Introducer Needle: Echogenic 18 Ga. x 2.5 (6.35cm) XTW and 5mL ArroW Raulerson Spring-Wire Introduction Syringe; however, the kit contains, and should state, Introducer Needle: 18 Ga. x 2.5 (6.35cm) XTW and 5mL ArroW Raulerson Spring-Wire Introduction Syringe. As a result of this labeling inconsistency, if the clinician were to place the needle under x-r