Reported Oct 7, 2020 · Terminated
KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.
Cardinal Health 200, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Cardinal Health 200, LLC · 785 Fort Mill Hwy · Fort Mill, SC · 29707-7555
Is this the product you have?
- KIT
- PRE OP DRAH - Product UsagePreoperative kit used to decolonize intranasal S. aureus
- Lot codes and dates
- ModelORPDH5994A
- Lot numbers
558357561502566549571467574058
- Expiration datesVaries by kit components
- Amount recalled
- 9,150 kits
Where it was sold
- Nationwide
- NC
Why it was recalled
Only providing one nasal swab in our pre-operative kit instead of the 4 required for proper treatment.
This product could cause temporary or reversible health problems — stop using it.
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