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Medical Components, Inc Recalls
38 recalls on record · July 4, 2012 to March 17, 2021 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 29, 2017Medical DevicesFDA
Medical Components, Inc dba MedComp recalls 9.6F Plastic Dignity Mid-Sized CT Port w/Pre-Attached Silicone Catheter The CT Power Injectable Implantable Infusion Po
Hazard: The 9.6F port kits were packaged with the incorrect valved peelable introducer. The label states the kit contains a 10F valved peelable introducer. The kit is packaged with a 9F valved peelable introducer. The port lumen will not fit through the introducer during the insertion procedure.
June 15, 2016Medical DevicesFDA
Medical Components, Inc dba MedComp recalls Tearaway Introducer, Model # VS203, VS303, 510 K # 130687, packaged individually in a pouch, 5 pouches per carton, lot #
Hazard: This recall has been initiated due to the product labeled with the incorrect expiration date.
May 6, 2015Medical DevicesFDA
Medical Components, Inc dba MedComp recalls 9F Plastic Dual Port; The port systems are totally implantable vascular access devices. They consist of an injection por
Hazard: The dual port with catheters was not covered under FDA clearance.
April 8, 2015Medical DevicesFDA
Medical Components, Inc dba MedComp recalls Medcomp Duo-Flow 400XL Catheter, Hemo-Flow Catheter, SLX Catheter, Triple Lumen Infusion Catheter, CT rated PICC, Split
Hazard: Medcomp has initiated the recall of Duo-Flow 400XL Catheter, Hemo-Flow Catheter, SLX Catheter, Triple Lumen Infusion Catheter, CT rated PICC, Split Cath III, PC Split Cath III because the product shipped was out of specification. One BI (biological indicator) out of 21 on the sterilization load was out of specification.
February 18, 2015Medical DevicesFDA
Medical Components, Inc dba MedComp recalls Hemodialysis Catheters and PICCs: Product identification: MCDLTSL24P (SF X 24CM LT HEMO-CATH), MC061422 (14FX15CM SLX D
Hazard: Drug products contained within the kits may have been rendered ineffective by a duplicate sterilization process. The kits include one or more of the following drugs: 5ml ampule of lidocaine, 3ml Chloraprep one-step, 10ml pre-filled saline syringe, Hygea saline wipes, and 3ml tinted Chloraprep. No injuries or illnesses were reported.
September 10, 2014Medical DevicesFDA
Medical Components, Inc dba MedComp recalls Split Cath III Trays, 16F x 28CM Product Usage: The Split Cath III is indicated for use in attaining long term vas
Hazard: The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath III instead of 28CM.
March 6, 2013Medical DevicesFDA
Medical Components, Inc dba MedComp recalls REF CMS-CT6T225, 6F Triple Lumen CT PICC with M.S.T. Components Product Usage: Power injectable infusion PICC inser
Hazard: The affected product was packaged with the incorrect introducer needle. The kit label indicates a "safety" needle is included; the kits were packaged with a non-safety needle.
July 4, 2012Medical DevicesFDA
Medical Components, Inc dba MedComp recalls MRCTT80041 MedComp 8F Plastic Pro-Fuse(R) CT Low Profile Port with Attachable Chronoflex(R) Polyurethane Catheter. Po
Hazard: Product was packaged with the incorrect port and does not match the label. The kit is labeled as an 8F Low Profile Pro-Fuse CT Port. The kit contains an 8F Midsize Dignity CT Port.