Drug recall

Medline Adult Anesthesia Set, REF DYNJ39985G

FDA recall event 97650 · Class II · Medline Industries, LP

Key facts

Event ID 97650
Recall numbers Z-0137-2026
Recalling firm Medline Industries, LP
Product type Devices
Products Medline Adult Anesthesia Set, REF DYNJ39985G
Classification Class II
Status Ongoing
Voluntary or mandated Firm Initiated
Reason for recall Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.
Initiation date Sep 10, 2025
Report date Oct 22, 2025
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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