VariSoft Infusion Set, Single Use.
Reported: September 25, 2024 Initiated: July 23, 2024 #Z-3186-2024
Product Description
VariSoft Infusion Set, Single Use.
Reason for Recall
Specific VariSoftTM Infusion Sets were packaged using incorrect secondary packaging (boxes) branded "Trusteel Infusion Set".
Details
- Recalling Firm
- Unomedical A/S
- Distribution
- US Nationwide distribution in the state of California.
- Location
- Lejre
Frequently Asked Questions
What product was recalled? ▼
VariSoft Infusion Set, Single Use.. Recalled by Unomedical A/S.
Why was this product recalled? ▼
Specific VariSoftTM Infusion Sets were packaged using incorrect secondary packaging (boxes) branded "Trusteel Infusion Set".
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 25, 2024. Severity: Moderate. Recall number: Z-3186-2024.
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