Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported December 14, 2022
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.
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.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Medical Action Industries, Inc. 306 recalled Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; an… - a moderate-severity action.
Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; an… was recalled by Medical Action Industries, Inc. 306 in December 14, 2022. Reason: The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctl…. Check the official notice for the remedy. Verify recall #Z-0464-2023 with the FDA Devices before acting.
The recall
Medical Action Industries, Inc. 306 issued this moderate-severity FDA Devices recall-The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctl….
- Moderate
- severity level
- Class II
- classification
- December 14, 2022
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0464-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0464-2023) was formally reported on December 14, 2022, with the manufacturer initiating the action on October 12, 2022. It is classified under Moderate severity (Class II), with a current status of Terminated. Medical Action Industries, Inc. 306 is listed as the recalling firm, operating out of Arden, NC. Federal records list the affected scope as 24 cases (480 kits).
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: Distribution was made to MN. There was no foreign/government/military distribution.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
24 cases (480 kits)
Related Recalls
6
3 from same agency
Product description
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.
Reason for recall
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0464-2023 |
| Date reported | December 14, 2022 |
| Date initiated | October 12, 2022 |
| Recalling firm | Medical Action Industries, Inc. 306 |
| Firm location | Arden, NC |
| Affected scope | 24 cases (480 kits) |
| Distribution | Distribution was made to MN. There was no foreign/government/military distribution. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0464-2023) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Medical Action Industries, Inc. 306. Units affected: 24 cases (480 kits).
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 14, 2022. Severity: Moderate. Recall number: Z-0464-2023.
Where was the recalled product distributed? ▼
Distribution: Distribution was made to MN. There was no foreign/government/military distribution..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0464-2023) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported December 14, 2022. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.