DLP® 67312Recalls & reported problems
Medtronic, Inc. · CANNULA 67312 VEN RT METAL 12FR 10PK 17L · Class 2
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20613994879329), received between Jun 20, 2024 and Jun 20, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping Problem” (1 report).
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
- Jul 9, 2024Open, Classified
During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).
Z-3128-2024 · Root cause: Under Investigation by firm · FDA record ↗
- Mar 19, 2024Open, Classified
Potential for unsealed sterile packing.
Z-1805-2024 · Root cause: Process control · FDA record ↗
Most reported problems
Device problems
- Manufacturing, Packaging or Shipping Problem1
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.
MalfunctionJun 20, 2024Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF A DLP SINGLE STAGE VENOUS CANNULA WITH A RIGHT ANGLE METAL TIP, IT WAS REPORTED THAT AN INCORRECT DEVICE WAS PUT INTO THE PACKAGE. THE DEVICE WAS REPLACED. THERE WAS NO PATIENT INVOLVEMENT, SO NO ADVERSE EFFECT OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19573038 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.