Vein Pack, Vein Treatment II Pack, Vein Brunswick Pack, Vein No Lidocaine Pack, Vein Ablation Pack - contains Devon Light Glove Used during surgery

Class I - Dangerous

🏥 Medical Devices Recalled: April 20, 2015 Stradis Healthcare Other Medical Devices Nationwide

What Should You Do?

Check if you have this product:
Pack 682-949, 682-937, 682-900, 682-370, 682-218, 682-1264, 682-1529, 682-076, 682-192, 682-962, 682-968, 682-177, 682-394, 682-988, 682-156, 682-063, 682-151, 682-917, 682-250, 682-409, 682-960, 682-945, 682-218, 682-1264, 682-1412, 682-1422
Do not eat it: Even if it looks and smells fine, do not consume this product.
Throw it away or return it: You can return the product to the store for a full refund.
Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:: Stradis Healthcare, LLC.
Reason for Recall:: Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.
Classification:: Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
Status:: completed

Product Information

Full Description:

Vein Pack, Vein Treatment II Pack, Vein Brunswick Pack, Vein No Lidocaine Pack, Vein Ablation Pack - contains Devon Light Glove Used during surgery

Product Codes/Lot Numbers:

Pack 682-949, 682-937, 682-900, 682-370, 682-218, 682-1264, 682-1529, 682-076, 682-192, 682-962, 682-968, 682-177, 682-394, 682-988, 682-156, 682-063, 682-151, 682-917, 682-250, 682-409, 682-960, 682-945, 682-218, 682-1264, 682-1412, 682-1422