Skip to content

Ta TA3035S

by Covidien LP

Ta TA3035S is a Class II device made by Covidien LP, cleared under FDA 510(k) K231491 on 16 Aug 2023 (1 earlier submission) and listed in FDA GUDID since 2 Sep 2015 (UDI-DI 10884521043114), active as of 23 Oct 2026. 73 FDA recalls are linked to it.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

24 ongoing

This device is named in the recall

Documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK231491 Date16 Aug 2023DecidedStatusActive
United StatesGUDID listing Number10884521043114 UDI-DI Date2 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • FDA 510(k) K231491 decided 16 Aug 2023 Active· +1 more in the status table
  • FDA GUDID UDI-DI 10884521043114 listed 2 Sep 2015 Listed

Recalls

73 recalls · 24 ongoing · FDA

  • 9 recalls, same reason

    • Ongoing Z-0003-2021 FDA Class II initiated 12 Aug 2020
    • Ongoing Z-0009-2021 FDA Class II initiated 12 Aug 2020
    • Ongoing Z-0004-2021 FDA Class II initiated 12 Aug 2020
    • Ongoing Z-0007-2021 FDA Class II initiated 12 Aug 2020
    • Ongoing Z-0006-2021 FDA Class II initiated 12 Aug 2020
    • Ongoing Z-0001-2021 FDA Class II initiated 12 Aug 2020
    • Ongoing Z-0008-2021 FDA Class II initiated 12 Aug 2020
    • Ongoing Z-0002-2021 FDA Class II initiated 12 Aug 2020
    • Ongoing Z-0005-2021 FDA Class II initiated 12 Aug 2020

    The device staples may not properly form upon application preventing adequate hemostasis. Use of a product with this assembly error may result in incomplete staple formation.

  • 12 recalls, same reason

    • Ongoing Z-1832-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1834-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1828-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1826-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1827-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1836-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1833-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1835-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1830-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1825-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1829-2019 FDA Class II initiated 17 May 2019
    • Ongoing Z-1831-2019 FDA Class II initiated 17 May 2019

    The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.

  • 43 recalls, same reason

    • Ongoing Z-2503-2018 FDA Class II initiated 22 May 2018
    • Ongoing Z-2504-2018 FDA Class II initiated 22 May 2018
    • Ongoing Z-2505-2018 FDA Class II initiated 22 May 2018
    • Terminated Z-1826-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1840-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1821-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1820-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1858-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1819-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1838-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1854-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1818-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1815-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1825-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1847-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1862-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1855-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1829-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1844-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1842-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1824-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1837-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1828-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1859-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1848-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1830-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1817-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1843-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1831-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1863-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1823-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1833-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1849-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1839-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1814-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1850-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1852-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1832-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1816-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1865-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1822-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1866-2018 FDA Class II initiated 26 Apr 2018
    • Terminated Z-1834-2018 FDA Class II initiated 26 Apr 2018

    Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding or leakage of luminal contents.

  • 2 recalls, same reason

    • Completed Z-0748-2021 FDA Class II initiated 23 Nov 2020
    • Completed Z-0747-2021 FDA Class II initiated 23 Nov 2020

    May contain a damaged internal component which could impede staple deployment and result in incomplete staple formation and a non-functional staple line preventing adequate hemostasis, or leading to anastomotic leak, pneumothorax, tissue damage or other delayed secondary complications including infection, peritonitis, and sepsis

    • Terminated Z-1264-2020 FDA Class II initiated 17 Jan 2020

    Potential for the sterile barrier to be compromised. Products with a compromised sterile barrier may result in a potentially increased risk for infection

    • Terminated Z-0636-2018 FDA Class II initiated 13 Sep 2017

    Potential for failure of the device safety interlock. The safety interlock prevents an empty single-use loading unit from being fired a second time.

  • 4 recalls, same reason

    • Terminated Z-0819-2016 FDA Class II initiated 2 Dec 2015
    • Terminated Z-0821-2016 FDA Class II initiated 2 Dec 2015
    • Terminated Z-0820-2016 FDA Class II initiated 2 Dec 2015
    • Terminated Z-0822-2016 FDA Class II initiated 2 Dec 2015

    Staplers fail to fire or partially fire and reports of the instrument articulating lever disengaging during use

    • Terminated Z-1063-2013 FDA Class II initiated 11 Feb 2013

    Single Use Loading Unit contained two staples loaded in each cartridge pocket and may result in difficulty firing and removing the device from the application site, which may require medical intervention

Timeline

76 dated events

  1. Recall initiated FDA recalls Z-0004-2021
  2. Recall initiated FDA recalls Z-0007-2021
  3. Recall initiated FDA recalls Z-0006-2021
  4. Recall initiated FDA recalls Z-0001-2021
  5. Recall initiated FDA recalls Z-0008-2021
  6. Recall initiated FDA recalls Z-0002-2021
  7. Recall initiated FDA recalls Z-0005-2021
  8. Recall initiated FDA recalls Z-0748-2021
  9. Recall initiated FDA recalls Z-0747-2021
  10. Cleared FDA 510(k) K231491

66 earlier events are in the sections above.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Ta
Generic name
Open-surgery manual linear stapler, single-use
Model / reference
TA3035S
Primary DI / UDI-DI
10884521043114
510(k) Number
FDA product code
GDW, GAG
GMDN term
Open-surgery manual linear stapler, single-use
Device class
Class II
Regulation number
878.4750, 878.4740
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Length — 30 Millimeter
Height — 3.5 Millimeter

Related devices

Category: Open-surgery manual linear stapler, single-use

Cleared under the same submission (K111825)

and 8 more cleared under K111825

Cleared under the same submission (K231491)

and 8 more cleared under K231491

Similar devices in this category

Other devices filed under Open-surgery manual linear stapler, single-use.

Other devices from Covidien LP

  • LigaSure MRASILF19

    Class II

  • Shiley 110860

    Class II

  • Shiley 110865

    Class II

  • Shiley 110870

    Class II

See all devices from Covidien LP →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)