Stradis Healthcare, LLC.: Medical Device Recall in 2015 - (Recall #: Z-1995-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product 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 Classification:

Class II

Date Initiated: April 20, 2015

Date Posted: July 15, 2015

Recall Number: Z-1995-2015

Event ID: 71130

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.

Status: Completed

Product Quantity: 55

Code Information:

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

Distribution Pattern:

Distribution US nationwide to AL, AK, CA, DE, FL, GA, HI, ID, IL, IN, KS, KY, ME, MD, MA, MI, MS, MO, NM, NJ, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA; Canada and Dubai

Voluntary or Mandated:

Voluntary: Firm initiated