PlainRecalls

Centurion Medical Products Corporation

Compiled from official public sources by the editorial team.

152 recalls on record · Latest: Jul 15, 2020

Centurion Medical Products Corporation Recall Insight

Centurion Medical Products Corporation appears on 152 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.149% 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 Jul 15, 2020, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 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 (50). The date window on this page runs from Aug 14, 2019 to Feb 12, 2020.

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 Feb 12, 2020

Centurion- Pathology Container 1150ST STERILE GRADUATED CONTAINER, 32 OZ. 17070 AI OR CARDIAC STERILE KIT 3703ST STERILE PATHOLOGY CONTAINER 3706…

FDA Devices Moderate Feb 12, 2020

Centurion-Irrigation Kit IG25STSS IRRIGATION GUN &VALVE SET W/SPLASHSHIELD Y

FDA Devices Moderate Feb 12, 2020

Centurion- SPEC0002B ARTHROGRAM TRAY SPEC0002B ARTHROGRAM TRAY SPEC0004C ARTHROGRAM TRAY SPEC0071B CUSTOM BX TRAY SPEC0076G STEREO BIOPSY PACK-L…

FDA Devices Moderate Feb 12, 2020

Centurion- Pelvic Exam Kits DYNDE1037 PELVIC EXAM TRAY,UNIVERSITY H 2019032090 DYNDE1037 PELVIC EXAM TRAY,UNIVERSITY H 2018091790

FDA Devices Moderate Feb 12, 2020

Centurion-LVAD Kits DM1005 DAILY LVAD MAINTENANCE KIT DM280A LVAD MANAGEMENT SYSTEM 2-7 DM320 PERCUTANEOUS LEAD MANAGEMENT KIT DM380 DAILY LVAD K…

FDA Devices Moderate Nov 27, 2019

NOSEBLEED TRAY Kit Code: MNS3885

FDA Devices Moderate Nov 27, 2019

EPISTAXIS TRAY Kit Code: MNS10165

FDA Devices Moderate Nov 27, 2019

YNHH SCOPE KIT Kit Code: MNS10475

FDA Devices Moderate Nov 13, 2019

Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - REG Code: DT11955

FDA Devices Moderate Nov 6, 2019

PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817

FDA Devices Moderate Nov 6, 2019

Maintenance Flush Kit/Blood Draw Product Code: DT19335

FDA Devices Moderate Nov 6, 2019

Kit, Port Access Product Code: DYNDC1582A

FDA Devices Moderate Nov 6, 2019

Port full Access Tray Product Code: DT19330

FDA Devices Moderate Oct 16, 2019

PEDIATRIC PICC INSERTION TRAY CVI4450A

FDA Devices Moderate Oct 16, 2019

OR VANTEX 7FR 3L 16CM CVC ECVC6665

FDA Devices Moderate Oct 16, 2019

PICC Line Accessory Kit CVI4285

FDA Devices Moderate Oct 16, 2019

NEONATAL PROCEDURE TRAY PICC CATHETERS CVI4535

FDA Devices Moderate Oct 16, 2019

Neonatal Cap Change Kit DT20315

FDA Devices Moderate Oct 16, 2019

CVC BUNDLE, 20CM, 3L, PI ECVC5120

FDA Devices Moderate Oct 16, 2019

Cap Change Kit DT20310

FDA Devices Moderate Oct 16, 2019

CVC BUNDLE MULTIMED, 3L, 20CM ECVC6060

FDA Devices Moderate Oct 16, 2019

CVC INSERTION BUNDLE 8.5FR 4L 16CM ECVC6355

FDA Devices Moderate Oct 16, 2019

CVC BUNDLE WITHOUT CATH CVI4600

FDA Devices Moderate Oct 16, 2019

CVC TRIPLE LUMEN SAFETY BUNDLE ECVC6070

FDA Devices Moderate Oct 16, 2019

CVC BUNDLE VANTEX 7F, 3L, 20CM ECVC6065

FDA Devices Moderate Oct 16, 2019

TRIPLE LUMEN CVC 20CM BUNDLE STCVC2040

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 Oct 16, 2019

Centurion CIRCLAMP W/1.1CM 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

UVC TRAY UVT875

FDA Devices Moderate Oct 16, 2019

IV START KIT IV8440

FDA Devices Moderate Oct 16, 2019

VANTEX 7FR, 16CM, 3L CVC BUNDLE ECVC6670

FDA Devices Moderate Oct 16, 2019

PORT AND IO ACCESS DRESSING KIT DT15780A

FDA Devices Moderate Oct 16, 2019

CENTRAL LINE BUNDLE ECVC6375

FDA Devices Moderate Oct 16, 2019

IV KIT - SORBAVIEW IVS3475

FDA Devices Moderate Oct 16, 2019

CAP BUNDLE KIT DYNDC2137

FDA Devices Moderate Oct 16, 2019

PEDIATRIC PICC INSERTION TRAY CVI4450

FDA Devices Moderate Oct 16, 2019

CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840

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.

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Data Sources

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.