Vial Adapter 8072050Recalls & reported problems
West Pharma. Services Il, . Ltd · Vial Adapter 20mm ML Blue SIL- SF · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07290108241075), received between Oct 10, 2022 and Feb 12, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Delivered as Unsterile Product” (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
- Appropriate Device Problem Term/Code Not Available1
- Delivered as Unsterile Product1
- Device Damaged Prior to Use1
- Particulates1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 12, 2025Delivered as Unsterile Product; Device Damaged Prior to Use; Delivered as Unsterile Product; Device Damaged Prior to Use
THE CUSTOMER, BAXTER HEALTHCARE CORPORATION, CONTACTED THE DEVICE MANUFACTURER ON 16JAN2025 TO REPORT THAT UPON INCOMING INSPECTION AT THE CUSTOMER SITE. LOT K513 WAS INSPECTED AND IT WAS NOTICED THAT SOME OF THE VIAL ADAPTER DEVICES WERE DEFORMED AND STUCK TOGETHER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21367727 ↗MalfunctionOct 10, 2022Particulates; Appropriate Device Problem Term/Code Not Available; Particulates; Appropriate Device Problem Term/Code Not Available
ON (B)(6) 2022, BAXTER HEALTHCARE CORPORATION (BAXTER) CONTACTED (B)(4) TO REPORT A FOREIGN MATERIAL ADHERED TO THE INSIDE OF THE SEALED PACKAGING OF (B)(4) VIAL ADAPTER (CATALOG# 8072050, LOT F645). THIS ISSUE WAS FOUND BY BAXTER ON ONE VIAL ADAPTER DURING THEIR INSPECTION OF 10,900 VIAL ADAPTERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15573258 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.