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U.S. Department of Health and Human Services

Class 2 Device Recall Ray TFC Device with End Caps

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 Class 2 Device Recall Ray TFC Device with End Capssee related information
Date Initiated by FirmAugust 18, 2008
Date PostedOctober 20, 2008
Recall Status1 Terminated 3 on November 04, 2008
Recall NumberZ-0151-2009
Recall Event ID 49439
PMA NumberP950019 
Product Classification Intervertebral Fusion Device with Bone Graft - Product Code MAX
ProductRay TFC Device with End Caps: Single Patient use; Sterile; Stryker Spine Ray Cage 7-2021 20 (catalog #) mm diameter x 21 mm long. Ray Cages are indicated for use with autogenous bone graft in patients with Degenerative Disc Disease (DDD) at one or two levels for L2 to S1.
Code Information Lot code 07A259
Recalling Firm/
Manufacturer		 Stryker Spine
2 Pearl Ct
Allendale NJ 07401-1611
For Additional Information ContactSusan Krasny, Ph.D., RAC
201-760-8150
Manufacturer Reason
for Recall		The label on one side on the Ray TFC Device (Ray Cage) is incorrect. It reads 20 mm x 26 mm instead of 20 mm x 21 mm.
FDA Determined
Cause 2		Labeling mix-ups
ActionUrgent Product Recall notification letters were sent via Fed Express on August 18, 2008 to Stryker Branches and Hospital Risk Managers. The firm asked customers to examine their inventory and hospital locations to identify the product; reconcile all products on the Product Accountability Form and attached distribution sheet; and fax a copy of the Accountability Form and distribution sheet to Sarah Thompson within 5 days of receipt of the notice. All questions are to be directed to Susan Krasny at 201-760-8150.
Quantity in Commerce69 units
DistributionNationwide Distribution
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
PMA DatabasePMAs with Product Code = MAX
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