Micro Therapeutics, Inc. Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only
Brand
Micro Therapeutics, Inc.
Lot Codes / Batch Numbers
Lot # B262322 UDI: (00) 847536005983
Products Sold
Lot # B262322 UDI: (00) 847536005983
Micro Therapeutics, Inc. is recalling Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only due to Outer carton packaging of microcatheters were exposed to wet substance during transport.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Outer carton packaging of microcatheters were exposed to wet substance during transport.
Recommended Action
Per FDA guidance
On June 30, 2022, Micro Therapeutics, Inc. issued a "URGENT: MEDICAL DEVICE RECALL (REMOVAL)" to affected customers. The recall notification ask consignees to take the following actions: 1. Do NOT use any impacted product. Remove and quarantine all unused impacted product in your inventory. 2. Return the impacted products to Medtronic. Your Medtronic representative may assist in facilitating the return of product, as necessary. If alternative product is needed, your Medtronic representative can assist you with identifying a suitable replacement product. 3. Complete and return the Customer Confirmation Form enclosed in this letter acknowledging that you have received this information. 4. This communication needs to be passed to all those who need to be aware within your organization where impacted devices have been transferred, and to any other associated organizations that may be impacted by this action. 5. Adverse reactions or quality problems experienced with this product should be reported to Medtronic and FDA MedWatch Adverse Event Reporting program via: " Medtronic Quality Assurance at rs.nvcomplaints@medtronic.com or call +1 (763) 514-4000 (Worldwide) " The FDA website (http://www.fda.gov/Safety/MedWatch/HowtoReport/default.htm) or call FDA at 1-800-FDA-1088.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026