Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medical Action Industries Inc. Port Access Kit Recalled by Medical Action Industries, Inc. 306 Due to The Port Access Kits were incorrectly labeled as...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medical Action Industries, Inc. 306 directly.
Affected Products
Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries Inc. IV Start Kit, REF #78019 (on kit label), sterile. Kit components are the Port Access Kit.
Quantity: 24 cases (480 kits)
Why Was This Recalled?
The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctly labeled as Port Access Kits.
Where Was This Sold?
This product was distributed to 1 state: MN
About Medical Action Industries, Inc. 306
Medical Action Industries, Inc. 306 has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report