ClearanceBrief
Recall Z-1378-2008 ยท LXH Orthopedic Manual Surgical Instrument

Stryker Spine

Radius Capspin is a non-sterile instrument for use with other devices in spinal surgery.

DateAug 19, 2008 (initiated Feb 19, 2008)
StatusTerminated
ReasonThe Radius Capsin has separation of the tip from the inserter.
Root causeDevice Design
ActionRecall notification was sent via FedEx on February 19, 2008 to all branches/agencies. All questions are to be directed to Michelle Klein, Regulatory Compliance Specialist - 201-760-8256.
Quantity52
DistributionProduct was distributed to a limited population during a product launch for the purposes of gathering feedback on the product.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.