KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.
Reported: October 7, 2020 Initiated: July 30, 2020 #Z-3016-2020
Product Description
KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.
Reason for Recall
Only providing one nasal swab in our pre-operative kit instead of the 4 required for proper treatment.
Details
- Recalling Firm
- Cardinal Health 200, LLC
- Units Affected
- 9,150 kits
- Distribution
- US Nationwide distribution including the state of North Carolina.
- Location
- Fort Mill, SC
Frequently Asked Questions
What product was recalled? ▼
KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.. Recalled by Cardinal Health 200, LLC. Units affected: 9,150 kits.
Why was this product recalled? ▼
Only providing one nasal swab in our pre-operative kit instead of the 4 required for proper treatment.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 7, 2020. Severity: Moderate. Recall number: Z-3016-2020.
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