Stradis Healthcare Recalls Podiatry Packs Containing Recalled Devon Light Gloves
Stradis Healthcare is recalling Podiatry Packs because they contain Devon Light Gloves that are subject to a separate recall by Medtronic.
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 measure triggered by a component recall from the manufacturer, with no specific injuries or illnesses reported in the source text.
Plain-English summary
Stradis Healthcare, LLC. is recalling Podiatry Packs that contain Devon Light Gloves. The recall is being conducted because the manufacturer of the gloves, Medtronic, has recalled the Devon Light Glove component.
The affected product is a convenience kit used during surgery. The recall covers four specific pack codes: 888-2378, 888-2411, 888-2429, and 888-2553. These products were distributed nationwide in the United States to specific states, as well as to Canada and Dubai.
Consumers and healthcare facilities should stop using these specific Podiatry Packs and contact Stradis Healthcare for further instructions regarding the recall.
The recalled product
- Product
- Podiatry Pack - contains Devon Light Glove Used during surgery
- Manufacturer
- Stradis Healthcare, LLC.
- Category
- Medical Device — Surgical Kits
- Hazard
- Affected units
- 4
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 (4)
- Pack 888-2378
- 888-2411
- 888-2429
- 888-2553
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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