CLASS II ONGOING Device recall · Reported 24 Aug 2022 · FDA Enforcement Report

Echelon -14, 45 Tip Shape recalled by Micro Therapeutics

Micro Therapeutics is recalling Echelon -14, 45 Tip Shape, distributed nationwide in the US. The recall was initiated on 30 Jun 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # B177543 UDI: (00) 847536006270
Quantity recalled8 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-1556-2022
FDA event ID
90622
Recalling firm
Micro Therapeutics, Irvine, CA
Classification
Class II
Status
Ongoing
Recall initiated
30 Jun 2022
FDA classified
18 Aug 2022
Reported
24 Aug 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Packaging Defects

Timeline

30 Jun 2022Recall initiated by company
18 Aug 2022Classified by FDA+49 days
24 Aug 2022Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Outer carton packaging of microcatheters were exposed to wet substance during transport.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only

Where it was distributed

US Nationwide Distribution: None OUS: Brazil

Nationwide

Questions about this recall

Why was it recalled?

Outer carton packaging of microcatheters were exposed to wet substance during transport.

Which lots are affected?

Lot # B177543 UDI: (00) 847536006270

Where was it sold?

US Nationwide Distribution: None OUS: Brazil

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 90622
ReportedClassRecallCompanyReasonWhere
CLASS IIEchelon -14 Micro Catheter recalled by Micro TherapeuticsMicro TherapeuticsPackaging DefectsNationwide

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