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device recall
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BALT USA, LLC device recall (Cls I)

September 25, 2025updated 5mo ago
community read0 votes

Brand Name: MEGA Ballast Distal Access Platform Product Name: Mega Ballast Model/Catalog Number: MEGABT09180, MEGABT09190, MEGABT091100, MEGABT091110 Software Version: N/A Product Description: The Mega Ballast 091 is designed with a semi-rigid proximal shaft and a highly flexible distal shaft. The design facilitates the advancement of the Mega Ballast to access the tortuous vasculature over a guidewire and a respective dilator. The outer surface of the Mega Ballast is coated with a hydrophilic coating to facilitate lubricity from tip to 40 cm proximal. The proximal end of the Mega Ballast incorporates a Luer fitting hub for the attachment of accessories. The Mega Ballast is provided sterile, non-pyrogenic, and is intended for single use only. Component: Not a component — Reason: Due to an identified manufacturing defect involving coating material lifting within the catheter's distal inner diameter/lumen. — Status: Ongoing

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same company · ±60 days · 3

  • device 510kBalt USA, LLC — Optima Coil System (Optima Packing Coil System) (510k cleared)Sep 26, 2025
  • device 510kBalt USA, LLC — Carrier XL Delivery Catheter (510k cleared)Oct 22, 2025
  • approvalLYNKUET (ELINZANETANT) — FDA approvalOct 24, 2025

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