Class IIOngoingZ-1913-2026
ARROW INTERNATIONAL, LLC recalls FLEXTIP PLUS EPIDURAL CATHETER
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
ARROW INTERNATIONAL, L…NCApr 29, 2026
Recalls: Process control
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 157–168 of 816 recalls
Class IIOngoingZ-1912-2026
ARROW INTERNATIONAL, LLC recalls PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code:…
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
ARROW INTERNATIONAL, L…NCApr 29, 2026
Class IIOngoingZ-1911-2026
ARROW INTERNATIONAL, LLC recalls ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159…
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
ARROW INTERNATIONAL, L…NCApr 29, 2026
Class IIOngoingZ-1910-2026
ARROW INTERNATIONAL, LLC recalls Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)2…
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
ARROW INTERNATIONAL, L…NCApr 29, 2026
Class IIOngoingZ-1822-2026
THERAKOS DEVELOPMENT LIMITED recalls Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/…
Increased difficulty in installing the centrifuge bowl onto the centrifuge bowl holder. Improper installation may cause the centrifuge bowl to dislodge, resulting in a broken bowl during the prime cycle or treatment phas…
THERAKOS DEVELOPMENT L…Apr 22, 2026
Class IIOngoingZ-1812-2026
Wilson-Cook Medical Inc. recalls Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only
Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.
Wilson-Cook Medical In…NCApr 22, 2026
Class IIOngoingZ-1811-2026
ARJOHUNTLEIGH POLSKA Sp. Z.O.O. recalls Arjo Tenor mobile passive patient lift
An internal component of the actuators in a certain production batch may not meet the required mechanical strength. This could result, in the worst case scenario, in a sudden loss of the actuator's ability to hold the lo…
ARJOHUNTLEIGH POLSKA S…Apr 22, 2026
Class IIOngoingZ-1774-2026
Molded Products Inc recalls See Luer Cap Set
Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.
Molded Products IncIAApr 15, 2026
Class IIOngoingZ-1772-2026
Beckman Coulter, Inc. recalls MicroScan Neg MIC 3J REF C54814
Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics
Beckman Coulter, Inc.CAApr 15, 2026
Class IIOngoingZ-1704-2026
SUMMA THERAPEUTICS, LLC recalls Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Cathete…
Potential for the balloon in the device to not meet burst specifications.
SUMMA THERAPEUTICS, LL…MAApr 8, 2026
Class IIOngoingZ-1699-2026
Intuitive Surgical, Inc. recalls Brand Name: da Vinci S
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Intuitive Surgical, In…CAApr 8, 2026
Class IIOngoingZ-1698-2026
Intuitive Surgical, Inc. recalls Brand Name: da Vinci S
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Intuitive Surgical, In…CAApr 8, 2026