PlainRecalls

Centurion Medical Products Corporation

99 recalls on record · Latest: Feb 12, 2020

Centurion Medical Products Corporation Recall Insight

Centurion Medical Products Corporation appears on 99 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.118% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Feb 12, 2020, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 49 entries, severity tagging shows 1 critical, 48 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 47 of 49 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (49). The date window on this page runs from Dec 18, 2013 to Oct 16, 2019.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Oct 16, 2019

CVC BUNDLE, 20CM, 4L, PI ECVC5095

FDA Devices Moderate Oct 16, 2019

Centurion CIRCLAMP W/1.3 CM BELL-single-use, disposable instrument used to compress the foreskin of the penis during circumcision of a male infant. …

FDA Devices Moderate Oct 16, 2019

INVASIVE PROCEDURE TRAY MNS9510

FDA Devices Moderate Oct 16, 2019

CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545A

FDA Devices Moderate Oct 16, 2019

CVC BUNDLE, 20CM, 3L, PI ECVC5120A

FDA Devices Moderate Oct 16, 2019

INFUSA PORT KIT DYNDC1840E

FDA Devices Moderate Oct 16, 2019

CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545

FDA Devices Moderate Oct 16, 2019

IV SECUREMENT KIT IVS3405

FDA Devices Moderate Oct 16, 2019

CAP CHANGE KIT DYNDC1496B

FDA Devices Moderate Oct 16, 2019

STERILE CAP CHANGE KIT DYNDC1946B

FDA Devices Moderate Oct 16, 2019

TRIPLE LUMEN BUNDLE KIT ECVC1540

FDA Devices Moderate Oct 16, 2019

INFUSA PORT KIT DYNDC1840F

FDA Devices Moderate Aug 14, 2019

DRIVELINE MANAGEMENT SYSTEM 1 DAILY Kit Code: DT18440A - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for general pati…

FDA Devices Moderate Aug 14, 2019

DAILY DRIVELINE KIT Kit Code: DM940 - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for general patient population.

FDA Devices Moderate Aug 14, 2019

CIRCUMCISION TRAY Kit Code: CIT2245 - Product Usage: Kit is used for performing circumcision procedures on newborns.

FDA Devices Moderate Aug 14, 2019

STERILE GRAVES VAGINAL SPECULUM MEDIUM Kit Code # GVS10MST - Product Usage:The speculum is used to spread the walls of the vagina to facilitate exami…

FDA Devices Moderate Aug 14, 2019

LACERATION TRAY Kit Code: SUT18370 - Product Usage: Kit is used for laceration repairs for general population.

FDA Devices Moderate Aug 14, 2019

SNAG FREE SUTURE TRAY Kit Code: SUT14355 - Product Usage: Kit is used for laceration repairs for general population.

FDA Devices Moderate Aug 14, 2019

UNIVERSAL BLOCK TRAY Kit Code: MNS6645 - Product Usage: Kit is used for regional anesthesia nerve blocks for general population.

FDA Devices Moderate Aug 14, 2019

DRIVELINE MANAGEMENT TRAY Kit Code: DT17780B - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for general patient popula…

FDA Devices Moderate Aug 14, 2019

NEONATAL PICC INSERTION TRAY Kit Code: CVI2310 - Product Usage: Kit is used for Peripheral Central Line Insertion procedures on newborns.

FDA Devices Moderate Aug 14, 2019

LVAD DRESSING SYSTEM W/BIOPATCHKit Code: DM700 - Product Usage: Kit is used for Left Ventricular Assist Device Dressing System for general patient po…

FDA Devices Moderate Aug 14, 2019

HIGH DRAINAGE LVAD TRAY Kit Code: DM950 - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for general patient population.

FDA Devices Moderate Jun 12, 2019

Sterile Nail Clipper Concave Edge (67710)

FDA Devices Moderate Jun 12, 2019

Sterile Nail Nipper, Barrel Spring (I68400), Sterile

FDA Devices Moderate Mar 28, 2018

NEONATAL IV ACCESS SET

FDA Devices Moderate Mar 28, 2018

GENERAL PURPOSE INSTRUMENT TRAY

FDA Devices Moderate Mar 28, 2018

SUTURE REMOVAL TRAY, SET or KIT

FDA Devices Moderate Mar 28, 2018

LATEX FREE IV START SET

FDA Devices Moderate Mar 28, 2018

CATHETER SECUREMENT SYSTEM

FDA Devices Moderate Mar 28, 2018

NEONATAL IV START KIT

FDA Devices Moderate Mar 28, 2018

IV START KIT

FDA Devices Moderate Mar 28, 2018

INFANT IV SECUREMENT KIT

FDA Devices Moderate Mar 28, 2018

MINI PLASTICS SET

FDA Devices Moderate Mar 28, 2018

SorbaView Shield Dressing Change Tray

FDA Devices Moderate Mar 28, 2018

BLOOD DRAW KIT

FDA Devices Moderate Jan 10, 2018

SafetyGlide Needle, 22GA 1-1/2in, Catalog n. 301701, manufactured by BD, sold in Centurion Convenience Kits. Centurion component code BD17O1NS.

FDA Devices Moderate Apr 12, 2017

CUSTOM CADAVER KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-ste…

FDA Devices Moderate Apr 12, 2017

OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into n…

FDA Devices Moderate Apr 12, 2017

OPHTHALMIC DRS TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-…

FDA Devices Moderate Apr 12, 2017

POST-OP EYE TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-ste…

FDA Devices Moderate Apr 12, 2017

POST-OPERATIVE OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are t…

FDA Devices Critical Dec 14, 2016

Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The Multi-Med catheter is indicated for use in patients requiring administratio…

FDA Devices Moderate Jul 27, 2016

Convenience Kits from Centurion that contain a Medtronic/Covidien Light Glove ED SUTURE KIT VAGINAL DELIVERY TRAY ENDOSCOPY TRAY MINOR BASIN SET…

FDA Devices Moderate Mar 2, 2016

Convenience Kits from Centurion that contain an In-Vision- Plus Needleless IV Connector, Model: code RYM5001 InVision-Plus¿ Needless IV Connector…

FDA Devices Moderate Jan 14, 2015

Diagnostic Imaging Tray (General Surgery convenience kit)

FDA Devices Moderate Jan 14, 2015

Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)

FDA Devices Moderate Oct 1, 2014

0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in Centurion Convenience Kits. Recalled product …

FDA Devices Moderate Dec 18, 2013

Centurion Sterile # 84 Rubber Bands Reorder EB84, Caution: This product contains natural rubber latex which may cause allergic reactions. LATEX F…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds