Micro Therapeutics, Inc. recalls Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only
Outer carton packaging of microcatheters were exposed to wet substance during transport.
Read the official notice →- Date
- 2022-08-24
- Country
- United States
- Brand
- Micro Therapeutics
- Product
- Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only
- Classification
- Class II
- Units
- US Nationwide Distribution: None OUS: Brazil
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Micro Therapeutics recalls
- 2026-10-07
USMicro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 00763000448806 he Pipeline Flex Embolization…
Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter.
FDA · DeviceMicro Therapeutics, Inc.U.S. Nationwide distribution in the states of GA and TX.Official notice →- 2026-07-29
- US
Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300-20. Intracranial aneurysm flow diverter
Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm implants.
FDA · DeviceMicro Therapeutics, Inc.US Nationwide distribution in the states of CT, DE, IN, MA, NC, NJ, NM, NY,…Official notice → - 2025-03-12
- US
Micro Therapeutics, Inc. recalls Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-021-350-16, PED3-021-250-14, PED3-021-350-20,…
Use of embolization device with diameters greater-than-or-equal-to 4mm may lead to incomplete wall apposition and/or braid deformation (fish-mouthing/braid narrowing/braid collapse) noted during procedure and…
FDA · DeviceMicro Therapeutics, Inc.Worldwide distribution: US (nationwide): PR, OK, CA, MD, FL, NY, WA, MI, AL,…Official notice → - 2024-03-13
- US
Micro Therapeutics, Inc. recalls The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the infusion of the…
European version of microcatheter were distributed within US which contain a different "Indications for Use".
FDA · DeviceMicro Therapeutics, Inc.US Nationwide distribution in the states of AL, AZ, CA, CT, FL, GA, HI, IA,…Official notice → - 2022-06-22
- US
Micro Therapeutics, Inc. recalls AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System REF QC-10-30-3D;
Due to incorrect size and configuration labeling of the detachable coil system.
FDA · DeviceMicro Therapeutics, Inc.International distribution in the countries of China and Republic of Korea.Official notice →
Other drugs & medical recalls in the United States
- 2022-08-31
- US
Family Dollar Stores, Llc. recalls QP COUGH COLD TABLET 16 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
CGMP Deviations: product held outside appropriate storage temperature conditions.
- US
- 2022-08-24
- US
Siemens Medical Solutions USA, Inc recalls AXIOM Sensis or Sensis Vibe Combo systems as follows: System Material # AXIOM Sensis, Combo 64 6623974; AXIOM Sensis, Hemo…
The Sensis Signal Input Box provides hooks as a milled item on the bottom of the box support the possibility of mounting the Signal Input Box on an accessory rail (e.g., at the patient table), In the event the mounting…
FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide Distribution Foreign: Albania Algeria Angola Argentina Armenia…Official notice → - US
Becton Dickinson & Company recalls BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the…
Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.
FDA · DeviceBecton Dickinson & CompanyUS Nationwide Distribution CA FL GA IL MD MI OR PA PR TN TXOfficial notice → - US
Stradis Medical, LLC dba Stradis Healthcare recalls NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5"; Part Number: ZZ-0700
The sterile barrier may be compromised.
FDA · DeviceStradis Medical, LLC dba Stradis HealthcareUS Nationwide distribution in the state of SC.Official notice → - US
Trinity Sterile, Inc. recalls Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708
Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy
FDA · DeviceTrinity Sterile, Inc.US Nationwide distribution in the states of FL, PA.Official notice →