Summary
The FDA issued a Class II for VariSoft Infusion Set, Single Use. by Unomedical A/S. Reason: Specific VariSoftTM Infusion Sets were packaged using incorrect secondary packaging (boxes) branded "Trusteel Infusion Set"..
Details
Source
Device Recall
External ID
Z-3186-2024
Action Date
2024-09-25
Status
Ongoing
Category
device
Product Description
VariSoft Infusion Set, Single Use.
Lot/Code Info: UDI-DI: 05705244018747. Product Code: 1726035. Lot Number: 6005241
Reason for Recall
Specific VariSoftTM Infusion Sets were packaged using incorrect secondary packaging (boxes) branded "Trusteel Infusion Set".
Distribution
US Nationwide distribution in the state of California.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-23
Company
Lejre
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.
Unomedical A/S has 6 FDA actions in our database, including 6 recalls.
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 (Unomedical A/S) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Unomedical A/S have FDA actions?
Unomedical A/S has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-3186-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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