Medline Industries Inc recalls MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER, 8Fr, REF DYNCPE8
- Recall date
- October 10, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0112-2018
- FDA classification
- Class II
- Brand / firm
- Medline Industries Inc
- Sold / distributed
- FL, IN, TN, GA, NJ, UT, MD, Nicaragua, Honduras
Why it was recalled
Products labeled as sterile were distributed prior to sterilization
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER, 8Fr, REF DYNCPE8
Get recall alerts
Free email alert whenever Medline Industries Inc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Medline Industries Inc