McKesson 102-S60CRecalls & reported problems
Mckesson Medical-Surgical Inc. · SYRINGE 60 CC LUER LOCK Sterile · Class 2
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 20612479170302), received between Apr 14, 2024 and Aug 3, 2024 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (3 reports).
2 FDA recall records name this device's identifier, 2 still open.
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
Recalls naming this device
- Aug 6, 2024Open, Classified
The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has stated that these syringes lack FDA clearance and were inadvertently shipped due to an internal order processing error.
Z-3154-2024 · Root cause: Process control · FDA record ↗
- Jul 24, 2024Open, Classified
Affected syringes lack FDA clearance.
Z-2940-2024 · Root cause: Other · FDA record ↗
Most reported problems
Device problems
- Insufficient Device Problem Information3
- Environmental Particulates2
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 3, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
SYRINGE WAS BEING USED TO INJECT CHEMOTHERAPY INTO BAG AND LUER LOCK TIP BROKE OFF FROM SYRINGE, RESULTING IN SPILL INSIDE OF IV HOOD. SPILL WAS IMMEDIATELY CLEANED. EMPLOYEE'S PERSONAL PROTECTIVE EQUIPMENT WAS REPLACED. DRUG WAS WASTED AND DOSE WAS REMADE FOR PATIENT. CHEMICAL AGENT DID NOT REACH THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19901172 ↗MalfunctionApr 14, 2024Environmental Particulates; Environmental Particulates
THE CUSTOMER REPORT THAT HAIR IN SYRINGE AND RUPTURED SYRINGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102938 ↗MalfunctionApr 14, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
THE CUSTOMER REPORT THAT EACH SYRINGE PISTON AND BARREL CONTACT SURFACE, VISUALLY, HAS MOISTURE OR LUBRICANT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102936 ↗MalfunctionApr 14, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
THE CUSTOMER REPORT THAT THE SYRINGE BARREL RUPTURED, RESULTING IN DRUG LEAKAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102917 ↗MalfunctionApr 14, 2024Environmental Particulates; Environmental Particulates
THE CUSTOMER REPORT THAT THERE'S A HAIR IN THE SYRINGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102900 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.