Drug recall

DIEP FLAP Convenience kit, SKU DYNJ910120. Convenience kits used for various procedures.

FDA recall event 95806 · Class II · MEDLINE INDUSTRIES, LP - Northfield

Key facts

Event ID 95806
Recall numbers Z-0717-2025, Z-0718-2025, Z-0719-2025, Z-0720-2025, Z-0721-2025, Z-0722-2025, Z-0723-2025, Z-0724-2025, Z-0725-2025, Z-0726-2025
Recalling firm MEDLINE INDUSTRIES, LP - Northfield
Product type Devices
Products DIEP FLAP Convenience kit, SKU DYNJ910120. Convenience kits used for various procedures., FESS-MB PACK-LF Convenience kit, SKU DYNJ0888159I. Convenience kits used for various procedures.., KIT,SPINE LH Convenience kit, SKU DYNJ906448A., MAJOR NEURO PACK-LF Convenience kit, SKU DYNJ0578916X. Convenience kits used for various procedures., Medline brand, medical procedure convenience kits, labeled as: 1) CRANIOTOMY, SKU CDS982719X; 2) MVFF/FIBU #54-RF, SKU DYNJ21927Q; 3) MVFF/FIBU #54-RF, SKU DYNJ21927S; 3) NEURO PEDIATRIC, SKU… and 5 more
Classification Class II
Status Ongoing
Voluntary or mandated Firm Initiated
Reason for recall Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman…
Initiation date Nov 6, 2024
Report date Jan 1, 2025
City Northfield
State IL
Country United States
FEI number 1417592

At a glance

  • 10–99 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

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