Recall of Signia Tri-Staple Surgical Devices Due to Missing Pin Components
Covidien LLC is recalling Signia Tri-Staple 2.0 devices because missing pin components may cause incomplete staple formation, potentially leading to serious surgical complications.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II and involves a defect that can lead to serious medical complications such as sepsis, peritonitis, and pneumothorax, meeting the criteria for a Severe rating.
Plain-English summary
The U.S. Food and Drug Administration (FDA) has issued a Class II recall for the Signia Tri-Staple 2.0 Curved Tip 45mm Medium/Thick devices (model SIG45CTAMT) manufactured by Covidien LLC. The recall involves 3,113,280 units that were distributed domestically and internationally.
The recall is due to a defect where the device may be missing one of two pin components that maintain the alignment of the device jaws. This defect can result in incomplete staple formation during use. Incomplete staple formation may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax, which can result in the potential for infection and/or sepsis.
Healthcare facilities and distributors should stop using the affected devices and contact the recalling firm for instructions on return or replacement. The specific lot codes affected are listed in the source metadata.
The recalled product
- Product
- SIGNIA TRI-STAPLE 2.0 CURVED TIP 45MM MEDIUM/ THIC , SIG45CTAMT
- Manufacturer
- Covidien LLC
- Affected units
- 3,113,280
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 12 recalled by Covidien 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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