MIXJECT 9070103Recalls & reported problems
West Pharma. Services Il, . Ltd · MIXJECT™ 20mm w/20G x 1½" Needle · 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 07290108240832), received between Jul 21, 2023 and Jul 21, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination” (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.
Most reported problems
Device problems
- Contamination1
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 21, 2023Contamination; Contamination
THE CUSTOMER, GP PHARM, CONTACTED WEST PHARMA. SERVICES, IL LTD. (WEST IL) ON 22JUN2023 TO REPORT THAT DURING PACKAGING AND QUALITY CONTROL OF BATCH 230173, LOT F967, ONE UNIT OF THE MIXJECT 20MM W/20G X 1.5" NEEDLE WAS FOUND WITH A PARTICLE INSIDE OF THE PACKAGED DEVICE. THE EVENT WAS DISCOVERED PRIOR TO PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17373215 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.