Medline Debridement Tray, Sterile, Single Use Only. Assembled in USA by Medline Industries, Inc., Mundelein, IL 6060
Reported: February 7, 2018 Initiated: September 21, 2017 #D-0300-2018
Product Description
Medline Debridement Tray, Sterile, Single Use Only. Assembled in USA by Medline Industries, Inc., Mundelein, IL 6060
Reason for Recall
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Details
- Recalling Firm
- Medline Industries Inc
- Units Affected
- 90 cases
- Distribution
- Nationwide USA, Puerto Rico, China, Chile, Guam, Honduras, India, Israel, Malaysia, Mexico, Turkey
- Location
- Northfield, IL
Frequently Asked Questions
What product was recalled? ▼
Medline Debridement Tray, Sterile, Single Use Only. Assembled in USA by Medline Industries, Inc., Mundelein, IL 6060. Recalled by Medline Industries Inc. Units affected: 90 cases.
Why was this product recalled? ▼
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 7, 2018. Severity: Moderate. Recall number: D-0300-2018.
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