International Medical Devices Database

Manufacturer Address
Efoora, Inc. dba Virotek, L.L.C., 900 Asbury Dr, Buffalo Grove IL 60089-4557
Source
USFDA
2 Events
- Recall of Device Recall Virotek SAFELET 2.0 mm Safety Lancets
- Recall of Device Recall Virotek SAFELET 1.0 mm Safety Lancets

2 devices in the database

Device Recall Virotek SAFELET 2.0 mm Safety Lancets

Model / Serial
stock code 5000052, 5000101and 5000115, lot numbers 0018, 0023, 0024, 0025, 0026, 0027, 0028
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide and internationally to Australia, Belgium, Bolivia, Colombia, Finland, Israel, Italy, Japan, Mexico, Nigeria, Russia, Singapore, South Africa, Spain, Sweden, Taiwan, Trinidad, United Kingdom and Zimbabwe.
Product Description
Virotek SAFEL*E*T 2.0 mm Safety Lancets, 2.0 mm depth, stock code 5000052, packaged in single unit blister packs, 200 per box, 6 boxes per carton, stock code 5000101, packaged in single unit blue cap packaging, 100 per box, and stock code 5000115, packaged in single unit blue cap packaging, 200 per box; Virotek, L.L.C., 900 Asbury Dr., Buffalo Grove, IL 60089

Device Recall Virotek SAFELET 1.0 mm Safety Lancets

Model / Serial
stock code 5000052, lot numbers 0013, 0014, 0015, 0016, 0017, 0019, 0021
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide and internationally to Australia, Belgium, Bolivia, Colombia, Finland, Israel, Italy, Japan, Mexico, Nigeria, Russia, Singapore, South Africa, Spain, Sweden, Taiwan, Trinidad, United Kingdom and Zimbabwe.
Product Description
Virotek SAFEL*E*T 1.0 mm Safety Lancets, 1.0 mm depth, stock code 5000052, packaged in single unit blister packs, 150 or 200 per box, 6 boxes per carton; Virotek, L.L.C., 900 Asbury Dr., Buffalo Grove, IL 60089

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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Efoora, Inc. dba Virotek, L.L.C.

2 devices in the database

Device Recall Virotek SAFELET 2.0 mm Safety Lancets

Device Recall Virotek SAFELET 1.0 mm Safety Lancets