Medline Industries, LP recalls Medline convenience kits labeled as: 1) LAVH
Kits contain a potentially contaminated component which were recalled by the manufacturer
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 13–24 of 4,896 recalls
Kits contain a potentially contaminated component which were recalled by the manufacturer
Kits contain a potentially contaminated component which were recalled by the manufacturer
Kits contain a potentially contaminated component which were recalled by the manufacturer
Kits contain a potentially contaminated component which were recalled by the manufacturer
Kits contain a potentially contaminated component which were recalled by the manufacturer
Kits contain a potentially contaminated component which were recalled by the manufacturer
Kits contain a potentially contaminated component which were recalled by the manufacturer
Kits contain a potentially contaminated component which were recalled by the manufacturer
Kits contain a potentially contaminated component which were recalled by the manufacturer
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar Hemodialysis machines.
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.