Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact ARROW INTERNATIONAL, LLC or your healthcare provider for instructions. Notification method: Letter
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Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 This device is intended for injection or aspiration of fluids. The needle protection device covers the needle after use to help prevent needle sticks.. Reason: Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured. Classification: Class II. Quantity: 85. Distribution: U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.
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Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured