Alaris Medley LVP Bezel Assembly. Intended use to hold recall
Alaris Medley LVP Bezel Assembly. Intended use to hold platen assembly and help protect the bezel assembly's internal components from fluid intrusion.…
Why was Alaris Medley LVP Bezel Assembly. Intended use to hold recalled?
Administration of inappropriate quantities of fluid can result, with the potential to cause injury or death.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
P/N 49000204 Lot #'s 031815100, 032415100, 04061545 and 043015215
- Product
- Alaris Medley LVP Bezel Assembly. Intended use to hold platen assembly and help protect the bezel assembly's internal components from fluid intrusion.…
- Recalling firm
- Elite Biomedical Solutions LLC
- Quantity
- 346 units
- Distribution
- Nationwide Distribution in the states of AZ, CA, GA, IL, IN, KS, KY, MA, MD, MN, MO, MS, NC, NY, OH, PA, SC, TN, TX, VA & WI.
- Recall date
- August 26, 2015
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)