Stradis Upper Extremity Packs Recalled Due to Component Defect
Stradis Healthcare is recalling Upper Extremity Packs because they contain a Devon Light Glove component being recalled 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 source text does not specify the hazard or injury risk associated with the Medtronic component recall, nor does it report any illnesses or injuries. Per the rubric, this is treated as a precautionary recall without explicit high-risk pathogen or injury reports.
Plain-English summary
Stradis Healthcare, LLC. is recalling Upper Extremity Packs, which contain a Devon Light Glove used during surgery. The recall is being conducted because the manufacturer of the glove component, Medtronic, is recalling the Devon Light Glove.
The affected product is identified by Pack code 888-2606. The distribution pattern indicates the products were distributed nationwide in the United States to specific states, as well as to Canada and Dubai.
Consumers should stop using the affected Upper Extremity Packs and contact Stradis Healthcare or their supplier for further instructions regarding the recall.
The recalled product
- Product
- Upper Extremity Pack - contains Devon Light Glove Used during surgery
- Manufacturer
- Stradis Healthcare, LLC.
- Hazard
- Affected units
- 1
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 888-2606
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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