UnratedMedical device recall · FDA · Published November 4, 2022
Medical Action Industries Port a Cath Kit REF 586: Cardiac Catheter Kit Recall
Medical Action Industries recalls cardiac catheter introduction kits with REF 58647D. Affected units have specific lot numbers and UDI/DI codes. Consumers should contact the manufacturer for details.
Medical Action Industries is recalling cardiac catheter introduction kits with the reference number 58647D. This recall is due to potential safety issues with the product, though specific details about the hazard are not provided in the record. Read more at govinfonow.com/recall/59496-medical-action-industries-port-a-cath-kit-ref-586-cardiac.
“Medical Action Industries Port a Cath Kit REF 586: Cardiac Catheter Kit Recall.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59496-medical-action-industries-port-a-cath-kit-ref-586-cardiac. Based on FDA recall #Z-0751-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0751-2023%22&limit=1).
The FDA announced on November 4, 2022, that Medical Action Industries, Inc. is recalling its Port a Cath Kit REF 58647D cardiac catheter introduction kits. The agency classified the recall as Class II.
How to tell if you have it
Brand: Medical Action Industries
Product: Port a Cath Kit REF 58647D, cardiac catheter introduction kit
UDI/DI: 10809160156681
Lot Numbers: 297223, 297418
Quantity: 198 cases
Distribution: US Nationwide distribution in the state of VA
Context
GovInfoNow's records show Medical Action Industries, Inc. has 14 other recalls on record since December 2, 2019. Other recent recalls include a July 23, 2026 recall of Blood Culture Kits due to packaging seal risks and an Epidural Pain Kit recall for potentially compromised sterility. Medline Heart Cath Pack-LF Kits were recalled on March 24, 2026, for particulate risk, followed by Medline Medical Procedure Kits recalls on May 4, 2026, regarding catheter issues.
How to tell if you have this one
Check for the product reference number 58647D on the cardiac catheter introduction kit. Affected units have specific lot numbers: 297223 and 297418, and UDI/DI code 10809160156681.
Brand
Medical Action Industries
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Contact Manufacturer
Reach out to Medical Action Industries, Inc. 306 for specific instructions on how to handle the recalled product.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution in the state of VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3.4 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0751-2023 (November 4, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0751-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.