RecallRadar

FDA Device recall Z-1480-2015

Captiva's lumbar intervertebral fusion system Reamers (color code rings on the Reamers)

On 2015-04-29 the FDA classified a Class II recall of Captiva's lumbar intervertebral fusion system Reamers (color code rings on the Reamers) by Captiva Spine, citing it is possible for the titanium color-coded ring to detach from the Reamers.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1480-2015
ClassificationClass II
Statusterminated
Initiated2015-02-25
Published2015-04-29
Last updated2026-09-13 11:53 UTC
CompanyCaptiva Spine
DistributionAZ, CA, FL, GA, IN, NY, UT

Product

Captiva's lumbar intervertebral fusion system Reamers (color code rings on the Reamers).

Reason

It is possible for the titanium color-coded ring to detach from the Reamers.

Identifiers

code_info
Part #: PI-0507, Lot #s:1308811A, 1457704A; Part #: PI-0508, Lot #s: 1308812A, 1457705A; Part #: PI-0509, Lot #s: 10388…Part #: PI-0507, Lot #s:1308811A, 1457704A; Part #: PI-0508, Lot #s: 1308812A, 1457705A; Part #: PI-0509, Lot #s: 1038813A, 1457706A; Part #: PI-0510, Lot #s: 1308814A, 1457707A; Part #: PI-0511, Lot #s: 1308815A, 1457708A; Part #: PI-0512, Lot #s: 1308816A, 1457709A; Part #: PI-0513, Lot #s: 1308817A, 1457710A; Part #: PI-0514, Lot #s: 1308818A, 1457711A; Part #: PI-0507-S, Lot #: 2130005; Part #: PI-0508-S, Lot #: 2130006; Part #: PI-0509-S, Lot #: 2130007; Part #: PI-0510-S, Lot #: 2130008; Part #: PI-0511-S, Lot #: 2130009; Part #: PI-0512-S, Lot #: 2130010; Part #: PI-0513-S, Lot #:2130011; Part #: PI-0514-S, Lot #: 2130012

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1480-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.