Stradis Mississippi Pack Recalled Due to Medtronic Component Recall
Stradis Healthcare is recalling Mississippi Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is a precautionary action triggered by a component recall without specific reports of injury or illness in the source text, fitting the criteria for a voluntary precautionary recall.
Plain-English summary
Stradis Healthcare, LLC. is recalling the Mississippi Pack, a convenience kit used during surgery. The recall is initiated because the kit contains the Devon Light Glove, which is subject to a separate recall by its manufacturer, Medtronic.
The affected product is identified by Pack 682-1302. Distribution was nationwide in the United States to specific states including 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, and WA, as well as to Canada and Dubai.
Consumers and healthcare facilities should stop using the affected Mississippi Packs and contact Stradis Healthcare or Medtronic for instructions on return or replacement.
The recalled product
- Product
- Mississippi Pack - contains Devon Light Glove Used during surgery
- Manufacturer
- Stradis Healthcare, LLC.
- Category
- Medical Device — Surgical Kits
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Pack 682-1302
Distribution
Part of a larger recall action
This product is one of 51 recalled by Stradis Healthcare, LLC. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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