ClearanceBrief
Recall Z-1041-2024 ยท HCG Device, Neurovascular Embolization

BALT USA, LLC

Neurovascular embolization device. The Optima Coil System is a series specialized coils that are inserted into the vasculature under angiographic visualization to embolize intracranial aneurysms and other vascular anomalies. The system consists of an embolization coil implant comprised of platinum/tungsten, affixed to a delivery pusher to facilitate insertion into the hub of a microcatheter. The s

DateFeb 8, 2024 (initiated Jan 3, 2024)
StatusOpen, Classified
ReasonDiscoloration was identified along the delivery pusher which was attributed to corrosion of the hypotube. The material which caused the corrosion was identified as remnants of solder flux residue remaining on the hypotube component of the delivery pusher. Due to the location of the delivery pusher within the delivery system, it is possible for the discoloration to mechanically break off from the delivery pusher, leaving the potential for the material to flow through the delivery system (i.e. microcatheter), and into the patient vasculature causing foreign emboli.
Root causeMaterial/Component Contamination
ActionOn 01/03/2024, the firm sent an "URGENT: MEDICAL DEVICE RECALL" Letter via priority mail to customers informing them that Balt USA has became aware of a situation where discoloration along the delivery system pusher component of the Optima Coil System was identified during in-house inspection of released finished good products. The discoloration was observed on the outside of the PET jacket along the hypotube component. Customers are instructed to: 1) Stop or cease use of the affected recall product. 2) Inform their hospital staff, such as safety officers, pharmacists, purchasing agent, head
Quantity31785 coils
DistributionU.S.: AZ, CA, CO, FL, GA, HI, IL, KS, MA, ME, MO, MS, NC, NE, NH, NJ, NY, OH, OK, PA, SC, SD, TN, TX, VA, VT, WI and Puerto Rico O.U.S.: Argentina, Australia, Brazil, Canada, Chile, Columbia, Dominican Republic, Ecuador, France, Indonesia, India, Japan, Korea, Malaysia, Mexico, Panama, Paraguay, P
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K172390Optima Coil System
Blockade Medical, LLC (D.B.A. Balt Usa), Feb 18, 2018
K200030Optima Coil System
Balt USA, LLC, Feb 1, 2020
K223386Optima Coil System
Balt USA, LLC, Dec 6, 2022