Medline custom medical procedure kits labeled as: 1) UMC DR recalled over sterility concerns
- Recall date
- November 21, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476; 2) DIEP FLAP, REF DYNJ910…
- Recall number
- Z-0780-2025
- FDA classification
- Class II
- Brand / firm
- MEDLINE INDUSTRIES, LP - Northfield
- Sold / distributed
- Worldwide distribution - US Nationwide and the countries of UAE, and Canada.
Why it was recalled
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
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 custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476; 2) DIEP FLAP, REF DYNJ910120
Get recall alerts
Free email alert whenever MEDLINE INDUSTRIES, LP - Northfield has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: MEDLINE INDUSTRIES, LP - Northfield