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Centurion Medical Products Recalls
152 recalls on record · December 18, 2013 to July 15, 2020 · 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 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls PEDIATRIC IV & IV START KIT
Hazard: Convenience Kit containing components to assist practitioner with IV placement and securement.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls LATEX FREE IV START SET
Hazard: Convenience Kit containing components to assist practitioner with IV placement and securement.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls NEONATAL IV ACCESS SET
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls BLOOD DRAW KIT
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls INCISION & DRAINAGE TRAY or KIT
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls MINOR DRESSING CHANGE TRAY
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls TUBING CHANGE KIT
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls SorbaView Shield Dressing Change Tray
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls ST. CHRISTOPHER'S SECUREMENT SET
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls CATHETER SECUREMENT SYSTEM
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls CIRCUMCISION TRAY
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls MINI PLASTICS SET
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls GENERAL PURPOSE INSTRUMENT TRAY
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls SUTURE REMOVAL TRAY, SET or KIT
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
March 28, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls SKIN STAPLE REMOVER
Hazard: Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
January 10, 2018Medical DevicesFDA
Centurion Medical Products Corporation recalls SafetyGlide Needle, 22GA 1-1/2in, Catalog n. 301701, manufactured by BD, sold in Centurion Convenience Kits. Centurio
Hazard: Centurion is recalling specific lots of convenience kits, SafetyGlide Needle, 22GA 1-1/2in, manufactured by BD, sold in Centurion Convenience Kits. distributed between May 2016 and June 2017 due to notice received from BD's recall due to particulate that could be expelled out of the needle if used for injection.
April 12, 2017Medical DevicesFDA
Centurion Medical Products Corporation recalls CUSTOM CADAVER KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they
Hazard: Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.
April 12, 2017Medical DevicesFDA
Centurion Medical Products Corporation recalls OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer
Hazard: Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.
April 12, 2017Medical DevicesFDA
Centurion Medical Products Corporation recalls POST-OPERATIVE OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by
Hazard: Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.
April 12, 2017Medical DevicesFDA
Centurion Medical Products Corporation recalls EYE KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then
Hazard: Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.
April 12, 2017Medical DevicesFDA
Centurion Medical Products Corporation recalls OPHTHALMIC DRS TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; t
Hazard: Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.
April 12, 2017Medical DevicesFDA
Centurion Medical Products Corporation recalls OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufactur
Hazard: Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.
April 12, 2017Medical DevicesFDA
Centurion Medical Products Corporation recalls POST-OP EYE TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they
Hazard: Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.
December 14, 2016Medical DevicesFDA
Centurion Medical Products Corporation recalls Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The Multi-Med catheter is indicated for use in pat
Hazard: The kits contain Multi-Med Single Lumen Catheters that have a potential for excess material to remain at the tip of the catheter from the manufacturing process. It is possible that the excess material may separate from the catheter during use and pose a potential risk of embolism, which could result in serious injury or death.
July 27, 2016Medical DevicesFDA
Centurion Medical Products Corporation recalls Convenience Kits from Centurion that contain a Medtronic/Covidien Light Glove ED SUTURE KIT VAGINAL DELIVERY TRAY EN
Hazard: Kits from Centurion contain a Medtronic/Covidien Light Glove that is being recalled by the manufacturer, Medtronic. According to the notice received from Medtronic, the recall was initiated because some light covers may have splits or holes, which may result in the transfer of microorganisms from the light handle into the patient wound.
March 2, 2016Medical DevicesFDA
Centurion Medical Products Corporation recalls Convenience Kits from Centurion that contain an In-Vision- Plus Needleless IV Connector, Model: code RYM5001 InVisio
Hazard: Convenience Kits contain an In-Vision-Plus Needleless IV Connector, code RYM5001 that is being recalled by the manufacturer, RyMed Technologies, LLC. A component molding abnormality may cause female luer threads to crack, leading to potential for the mating tubing set to become detached and for the administration to be interrupted. Other components within these kits are not affected.
January 14, 2015Medical DevicesFDA
Centurion Medical Products Corporation recalls Pacemaker Tray (Cardiovascular Surgical Instruments convenience kit)
Hazard: According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hospira identified the particulate as human hair, embedded in and attached to a pinched area of the stopper.
January 14, 2015Medical DevicesFDA
Centurion Medical Products Corporation recalls Diagnostic Imaging Tray (General Surgery convenience kit)
Hazard: According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hospira identified the particulate as human hair, embedded in and attached to a pinched area of the stopper.
January 14, 2015Medical DevicesFDA
Centurion Medical Products Corporation recalls Nerve Block Tray (Nerve Block convenience kit)
Hazard: According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hospira identified the particulate as human hair, embedded in and attached to a pinched area of the stopper.
January 14, 2015Medical DevicesFDA
Centurion Medical Products Corporation recalls Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)
Hazard: According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hospira identified the particulate as human hair, embedded in and attached to a pinched area of the stopper.