What was recalled and why?

Angiodynamics, Inc. recalled AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (Pouch); Box Quantity: 5 pouches;. FDA's record states the reason for recall as: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.. The recall is logged under FDA recall number Z-1874-2026 with a Class II classification.

What should someone who has this product do?

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (Pouch); Box Quantity: 5 pouches;) and recall number Z-1874-2026, then follow Angiodynamics, Inc.'s recall instructions.

Has Angiodynamics, Inc. had other FDA recalls or enforcement actions?

Yes. Argus HQ has recorded 20 total FDA actions tied to Angiodynamics, Inc., including 20 recalls and 0 warning letters.

FDA Class II Recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21… by Angiodynamics, Inc.

Key facts

Recalling firm	Angiodynamics, Inc.
Manufacturer	Not disclosed in the FDA record.
Brand name	Not disclosed in the FDA record.
Product description	AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (Pouch); Box Quantity: 5 pouches;
Classification	Class II
Recall number	Z-1874-2026
Report date	Not disclosed in the FDA record.
Status	Ongoing
Reason for recall	The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.

In short: Angiodynamics, Inc. recalled AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (Pouch); Box Quantity: 5 pouches; on 2026-04-29. FDA classified this action as a Class II recall (recall number Z-1874-2026). Reason for recall: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.. Recall status: Ongoing. This is a device-category FDA recall record.

What this classification means

FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote. In this case, the recalling firm is Angiodynamics, Inc. and the affected product is described in FDA's record as: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (Pouch); Box Quantity: 5 pouches;. FDA's stated reason for the recall is: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.. The recall is tracked under FDA recall number Z-1874-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do. Recall status can change while FDA and the recalling firm continue corrective actions, so checking the firm's own notice for the most current guidance is recommended.

What consumers should do

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Specifically, check whether the product in your possession matches the description on file with FDA -- AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (Pouch); Box Quantity: 5 pouches; -- and the recall number Z-1874-2026. If it matches, stop using or distributing it and contact Angiodynamics, Inc. or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice.

Angiodynamics, Inc.’s FDA history

Argus HQ has recorded 20 total FDA actions tied to Angiodynamics, Inc.: 0 warning letters, 20 recalls, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

What was recalled and why?: Angiodynamics, Inc. recalled AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (Pouch); Box Quantity: 5 pouches;. FDA's record states the reason for recall as: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.. The recall is logged under FDA recall number Z-1874-2026 with a Class II classification.
How serious is this recall?: FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote.
What should someone who has this product do?: Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (Pouch); Box Quantity: 5 pouches;) and recall number Z-1874-2026, then follow Angiodynamics, Inc.'s recall instructions.
Has Angiodynamics, Inc. had other FDA recalls or enforcement actions?: Yes. Argus HQ has recorded 20 total FDA actions tied to Angiodynamics, Inc., including 20 recalls and 0 warning letters.

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Full FDA history for Angiodynamics, Inc.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). FDA Class II Recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21… by Angiodynamics, Inc. — Recall Details. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/recall/fda-recall-angiodynamics-inc-z-1874-2026

MLA

"FDA Class II Recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21… by Angiodynamics, Inc. — Recall Details." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/recall/fda-recall-angiodynamics-inc-z-1874-2026.

Chicago

Argus HQ Research. "FDA Class II Recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21… by Angiodynamics, Inc. — Recall Details." Digital Empire Holdings LLC. Accessed August 27, 2026. https://argushq.ai/recall/fda-recall-angiodynamics-inc-z-1874-2026.

BibTeX

@misc{argushq_argushq_ai_recall_fda_recall_angiodynamics_inc_z_1874_2026_2026,
  title = {FDA Class II Recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21… by Angiodynamics, Inc. — Recall Details},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/recall/fda-recall-angiodynamics-inc-z-1874-2026},
  note = {Accessed: August 27, 2026}
}

Source: FDA.gov — Recalls ↗