AVID TruCustom CATH PACK convenience kits recalled over foreign material
- Recall date
- June 22, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Avid Medical, Inc. recalls AVID TruCustom CATH PACK convenience kits, Item Code: LGHM036-14
- Recall number
- Z-0786-2018
- FDA classification
- Class II
- Brand / firm
- Avid Medical, Inc.
- Sold / distributed
- Distributed in 10 states: IL, KY, LA, MA, MO, NY, OH, TX, VA, WI.
Why it was recalled
Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
AVID TruCustom CATH PACK convenience kits, Item Code: LGHM036-14
Get recall alerts
Free email alert whenever Avid Medical, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Avid Medical, Inc.