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Serious recall: Injury is possible or has been reported. Take action promptly.

Micro Therapeutics, Inc. 2022-08-24 Health serious FDA
Health · FDA · Recall #FDA-Z-1556-2022

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

Issued August 24, 2022 · Micro Therapeutics, Inc.

In August 2022, Micro Therapeutics, Inc. recalled the Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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

What you should do

  1. 1 Stop using Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Micro Therapeutics, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Micro Therapeutics, Inc.
Category
Health
Recall date
August 24, 2022
Units affected
Not reported
Sold at
US Nationwide Distribution: None OUS: Brazil
Recall number
FDA-Z-1556-2022
Made in
United States
Issuing agency
FDA

In context

  • Micro Therapeutics, Inc. has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 870th Health recall we've logged in 2022.
Read the official FDA notice

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