McKesson 16-EP27010Recalls & reported problems
Mckesson Medical-Surgical Inc. · ELASTOMERIC PUMP 270MLX10ML/HR (10/CS) · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10612479271521), received between Jul 23, 2025 and Jul 23, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Failure to Deflate” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Deflate1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 23, 2025Failure to Deflate; Failure to Deflate
IT WAS REPORTED BY THE CUSTOMER THAT PATIENTS ARE HAVING ISSUES WITH GETTING DRUG TO INFUSE WHEN AN EXTENSION SET IS ATTACHED TO THEIR PICC LINE. NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURIES AS A RESULT OF THIS PRODUCT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22575324 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.