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Medline Industries Inc — Medline Pediatric IV Kit. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093
Check whether yours is affected, then follow the instructions below.
What’s wrong
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
The Recall Registry rates this serious — FDA Class II: temporary or medically reversible health harm.
What to do
Check the lot numbers below against what you have, and follow the FDA recall notice for what to do with the affected product. If you use it daily, or it is for a child, your pharmacist can tell you whether it matters and what to use instead.
Who to contact: Recalling firm: Medline Industries Inc
The product
Medline Pediatric IV Kit. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093
Details
- Units affected
- 50 cases
- Recall date
- September 21, 2017
- Brand
- Medline Industries Inc
Nationwide USA, Puerto Rico, China, Chile, Guam, Honduras, India, Israel, Malaysia, Mexico, Turkey
The official notice
This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.
Their exact wording: “Medline Industries Inc — Medline Pediatric IV Kit. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093”
Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.
Filed under: Children's medicine