Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
Summary
The FDA issued a Class II for Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312 by Medtronic Perfusion Systems. Reason: During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage .
Details
Source
Device Recall
External ID
Z-3128-2024
Action Date
2024-09-18
Status
Ongoing
Category
device
Product Description
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
Lot/Code Info: GTIN 20613994879329, Lot Numbers: 2023090954, 202312C065
Quantity Affected: 290 units
Reason for Recall
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).
Distribution
Worldwide distribution - US Nationwide and the countries of Cambodia, Greece, Ireland, Italy, Saudi Arabia, Switzerland, United Kingdom, Viet Nam.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-09
Company
Brooklyn Park, MN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 257 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Medtronic Perfusion Systems has 50 FDA actions in our database, including 49 recalls and 1 clearance.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Medtronic Perfusion Systems) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Medtronic Perfusion Systems have FDA actions?
Medtronic Perfusion Systems has 50 FDA actions in our database, including 49 recalls and 1 device clearance.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-3128-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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