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Recall Observatory FDA recall evidence

Device product

Reprocessed Agilis Steerable Introducer: indicated for introducing various cardiovascular catheters into the heart. (a) small curl (16.8mm curve type/71 cm length), Product Code STJ408309; (b) medium curl (22.4 mm curve type/71 cm length), Product Code STJ408310; (c) large curl (50 mm curve type/71 cm length), Product Code STJ408324

Z-0090-2019

September 17, 2018

Class II

Product summary

Firm
Sterilmed, Inc.
Event
Event 80999
Status
Terminated
Classification
Class II
Quantity
218 units
Official record key
device-enforcement:Z-0090-2019

Official wording

Reason: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements per product specification for biological residues determined by LAL testing.

Code information: All lots with expiration dates prior to 2019-06-08 of the following: (a) Product Code STJ408309, GTIN 10888551044912 (b) Product Code STJ408310, GTIN 10888551044929 (c) Product Code STJ408324, GTIN 10888551044950

Distribution pattern: U.S. Nationwide distribution in the states of CA, CO, MN, and WA.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    may not meet endotoxin requirements per product specification