Lower riskMedical device recall · FDA · Published July 6, 2020
Arrow Cannon II Plus Replacement Hub Set Recall: Incorrect Expiration Date Risk
Arrow recalls Cannon II Plus Replacement Hub Set with incorrect expiration dates on labels. Using expired products may increase infection risk. Consumers should check product codes and contact Arrow for details.
The lidstock states the incorrect expiration date for the product. This issue could result in use of a device that is expired which could potentially lead to an increased risk of infection or other complications. Sterility, biocompatibility, safety, or efficacy of the kits and their components are not assured beyond the correct expiration date.
Take action
Contact the company
📍Recalling firmArrow International Inc2400 Bernville Rd · Reading, PA 19605-9607
“Arrow Cannon II Plus Replacement Hub Set Recall: Incorrect Expiration Date Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64809-arrow-cannon-ii-plus-replacement-hub-set-recall-incorrect-expiration. Based on FDA recall #Z-2802-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2802-2020%22&limit=1).
The FDA announced on July 6, 2020, that Arrow International Inc. is recalling the Cannon II Plus Replacement Hub Set due to an incorrect expiration date on the lidstock. This error could lead to the use of expired devices, potentially increasing the risk of infection or other complications.
How to tell if you have it
Brand: Arrow
Product: Cannon II Plus Replacement Hub Set
Product Code: CAR-02400
Lot #: 13F19J0153 and 23F17H0547
The hazard
The lidstock states the incorrect expiration date for the product. This issue could result in use of a device that is expired which could potentially lead to an increased risk of infection or other complications. Sterility, biocompatibility, safety, or efficacy of the kits and their components are not assured beyond the correct expiration date.
Context
GovInfoNow's records show Arrow International Inc. has 52 other recalls on record since June 1, 2017. Other recent recalls include Arrow Arterial Kits and Trays (July 26, 2024), Arrow Ultra 8 IAB Catheter Kit (April 29, 2024), and ARROW QuickFlash Radial Artery Catheter (Feb. 12, 2024). Other recent recalls of similar products include Cardinal Health ChemoPlus Gowns Recall (Nov. 12, 2025), Arrow Medical Kits Recall (April 21, 2026), and B Braun Discofix Four Way Stopcock Recall (Aug. 4, 2026).
How to tell if you have this one
Check for product code CAR-02400 and lot numbers 13F19J0153 or 23F17H0547 on the hub set packaging or label. The product is intended for replacing damaged Cannon II Plus hub connections.
Brand
Arrow
Category
Medical device
FDA recall event · 4 products
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
World wide distribution
Recall number
Product, codes & lots
Z-2801-2020
Arrow Single Shot Epidural Anesthesia Kit - Product Usage: The Arrow Blunt Needle Single Shot Epidural Kit permits access to the epidural space.; Product Code: AK-03000-S Lot #: 13F17J0230
Z-2802-2020
Cannon II Plus Replacement Hub Set - Product Usage: is indicated for use in the replacement of a Cannon II Plus hub connection assembly that has been damaged.; Product Code: CAR-02400 Lot #: 13F19J0153 and 23F17H0547
Z-2803-2020
Arrow TheraCath Epidural Catheter - Product Usage: The Arrow Epidural Catheter permits access to the epidural space.; Product Code: EC-05000 Lot #: 13F18C0518
Z-2804-2020
NextStep Retrograde Replacement Hub Set - Product Usage: is indicated for use in the replacement of a NextStep Retrograde hub connection assembly that has been damaged.; Product Code: NRH-15192 Lot #: 13F19H0454
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for product code CAR-02400 and lot numbers 13F19J0153 or 23F17H0547 on the hub set.
How this recall unfolded
Recall timeline
FDA terminated this recall 16 months 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-2802-2020 (July 6, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2802-2020 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.