Drug recall

ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377

FDA recall event 95127 · Class II · MEDLINE INDUSTRIES, LP - Northfield

Key facts

Event ID 95127
Recall numbers Z-3069-2024, Z-3070-2024, Z-3071-2024, Z-3072-2024
Recalling firm MEDLINE INDUSTRIES, LP - Northfield
Product type Devices
Products ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377, ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377A, CRANIOTOMY PACK, Pack Number DYNJ46552O, KIT PEDI CRANI LAMI, Pack Number DYNJ907372A
Classification Class II
Status Ongoing
Voluntary or mandated Firm Initiated
Reason for recall A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that…
Initiation date Jun 18, 2024
Report date Sep 18, 2024
City Northfield
State IL
Country United States
FEI number 1417592

At a glance

  • 1–9 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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