Manifold Kit. Catalog Number K09-11867AP
Reported: November 30, 2016 Initiated: September 23, 2016 #Z-0632-2017
Product Description
Manifold Kit. Catalog Number K09-11867AP
Reason for Recall
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
Details
- Recalling Firm
- Merit Medical Systems, Inc.
- Units Affected
- 40 units
- Distribution
- Nationwide to VA, UT, and NC. Other foreign consignee Japan. No Canadian and VA/govt/military consignees.
- Location
- South Jordan, UT
Frequently Asked Questions
What product was recalled? ▼
Manifold Kit. Catalog Number K09-11867AP. Recalled by Merit Medical Systems, Inc.. Units affected: 40 units.
Why was this product recalled? ▼
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 30, 2016. Severity: Moderate. Recall number: Z-0632-2017.
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