FDAFDA · Food and drugs·Recall number D-0260-2018
Medline Pediatric IV Kit. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093
Published February 7, 2018 · Recall initiated: September 21, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Medline Industries Inc
- Distributor
- Nationwide USA, Puerto Rico, China, Chile, Guam, Honduras, India, Israel, Malaysia, Mexico, Turkey
- Lot
- Pack Number: DYKP1000A; Lots: 17AA2252
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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