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TEKTONA HV US Bone Cement

TECRES SPA · Model TEK-BC HV US-S · UDI-DI 08031497003351

NDN LOD Prescription

510(k) clearances

4,809

Adverse events (94 deaths)

Recalls

114

Facilities

Description

TEKTONA HV US Bone Cement is indicated for the treatment of pathological fractures of the vertebral body using a vertebroplasty or kyphoplasty procedure. TEKTONA HV US Bone Cement is a closed sysyem which containes the powder and liquid components separately. The device is disposable and sterile.

Recalls

Date	Firm	Reason
2022-12-15	TEKNIMED SAS	Incorrect expiry date. Product is labeled with expiry date 2027-02-28. The correct expiration date is 2025-02-28.
2021-05-18	Stryker Spine	The products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.
2021-05-18	Stryker Spine	The products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.
2021-03-25	Zavation	Products distributed as sterile may not have been adequately sterilized
2021-03-25	Zavation	Products distributed as sterile may not have been adequately sterilized
2021-03-25	Zavation	Products distributed as sterile may not have been adequately sterilized
2021-03-25	Zavation	Products distributed as sterile may not have been adequately sterilized
2021-03-25	Zavation	Products distributed as sterile may not have been adequately sterilized
2021-03-25	Zavation	Products distributed as sterile may not have been adequately sterilized
2021-03-25	Zavation	Products distributed as sterile may not have been adequately sterilized

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.