PlainRecalls

Cordis US Corp

Compiled from official public sources by the editorial team.

22 recalls on record · Latest: Apr 9, 2025

Cordis US Corp Recall Insight

Cordis US Corp appears on 22 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.022% 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 Apr 9, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 22 entries, severity tagging shows 15 critical, 7 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 22 of 22 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 (22). The date window on this page runs from Jul 20, 2022 to Apr 9, 2025.

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 Apr 9, 2025

Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only

FDA Devices Moderate Apr 9, 2025

Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only

FDA Devices Moderate Mar 19, 2025

Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of in…

FDA Devices Moderate Jan 17, 2024

MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites.

FDA Devices Moderate Jan 17, 2024

MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites

FDA Devices Critical Nov 15, 2023

Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE

FDA Devices Critical May 17, 2023

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC

FDA Devices Moderate Dec 21, 2022

Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.

FDA Devices Moderate Jul 20, 2022

PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX, PG3990BPS, PG3990BPX.

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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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.