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.
Reported: December 14, 2022 Initiated: October 12, 2022 #Z-0464-2023
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.
Details
- Recalling Firm
- Medical Action Industries, Inc. 306
- Units Affected
- 24 cases (480 kits)
- Distribution
- Distribution was made to MN. There was no foreign/government/military distribution.
- Location
- Arden, NC
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.
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