Signia Tri-Staple Surgical Device Recalled Due to Missing Pin Components
The FDA is recalling Signia Tri-Staple 2.0 devices because missing pin components may cause incomplete staple formation, 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 injuries 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 60mm Medium/Thick surgical stapler devices manufactured by Covidien LLC. The recall involves 3,113,280 units that were distributed nationwide and worldwide.
The recall was initiated because the devices 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 providers and facilities should stop using the affected devices and contact the manufacturer for instructions on return or replacement. The specific lot codes affected are listed in the official recall notice.
The recalled product
- Product
- SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC , SIG60CTAMT
- 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.
See all 12 products in this recall →Related recalls
Same manufacturer · Covidien LLC
See all →- ModerateEndoFLIP System Recall Due to Incorrect Catheter Expiration Flags
FDA (Devices) · 2026-08-26
- ModerateCovidien Shiley Disposable Decannulation Plug product labeling error
FDA (Devices) · 2026-07-08
- ModerateShiley tracheostomy tubes recalled over incorrect display box labeling
FDA (Devices) · 2026-06-10
- ModerateCovidien Mon-a-Therm general purpose temperature probes lack FDA clearance
FDA (Devices) · 2026-06-10
- ModerateCovidien esophageal stethoscope temperature sensors lack FDA clearance
FDA (Devices) · 2026-06-10
Same hazard · incomplete staple formation
See all →- SevereFDA Recalls Covidien TA Auto Suture Vascular Loading Units
FDA (Devices) · 2021-01-06
- SevereFDA Recalls Covidien TA Auto Suture Vascular Staplers Due to Damaged Components
FDA (Devices) · 2021-01-06
- HighEndo GIA Auto Suture Universal Loading Unit Recall for Staple Formation Defect
FDA (Devices) · 2020-10-07
- HighRecall of Covidien Endo GIA Universal Loading Units Due to Staple Formation Defect
FDA (Devices) · 2020-10-07
- SevereFDA Recalls Endo GIA Auto Suture Units Due to Staple Formation Defects
FDA (Devices) · 2020-10-07