Cordis US Corp recall records

22 reported ongoing

22 records in this archive. Latest source date Mar 4, 2025.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

Records and reported status

FDA device enforcement

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

Cordis became aware that the label for the carton box containing 10 units is incorrect for some boxes of two lots of MynxGrip. The carton box from lot F2322902 (Item MX5021, MynxGrip 5F) as labeled as lot F2322903 (MX6721, MynxGrip 6/7F) and product from lo...

Class IIReported ongoing

Distribution: US: NC, WV, TN, MS, MI, OH, CA

Official source for MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral...
FDA device enforcement

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

Cordis became aware that the label for the carton box containing 10 units is incorrect for some boxes of two lots of MynxGrip. The carton box from lot F2322902 (Item MX5021, MynxGrip 5F) as labeled as lot F2322903 (MX6721, MynxGrip 6/7F) and product from lo...

Class IIReported ongoing

Distribution: US: NC, WV, TN, MS, MI, OH, CA

Official source for MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femo...
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

Official source for ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM
FDA device enforcement

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

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement de...

Class IReported ongoing

Distribution: Worldwide distribution.

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

Reasons in these listed records

  • product mix-up; Vascular stent labeled as one size but contains a different size.
  • Catheter manufactured at the incorrect length.
  • Cordis became aware that the label for the carton box containing 10 units is incorrect for some boxes of two lots of MynxGrip. The carton box from lot F2322902 (Item MX5021, MynxGrip 5F) as labeled as lot F2322903 (MX6721, MynxGrip 6/7F) and product from lot F2322903 (MX6721, ...
  • Non-sterile product labeled as sterile was distributed.

These examples come from this result page and are not a ranking of every recall reason.

Checking Cordis US Corp

Is there a recall on cordis us corp right now?

This archive contains 22 records, including 22 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.

Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.

Where can I find older records?

Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

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