Spineart Recalls Tryptik 2 C-Plate Screws Due to Labeling Error
Spineart SA is recalling 8 units of Tryptik 2 C-Plate Self Tapping screws because the product labeling incorrectly displays a sketch of a self-drilling screw.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 1/5 (Low).
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is for a labeling error (incorrect sketch) with no reported injuries or illnesses, fitting the 'Low' severity criteria for documentation or packaging-only problems.
Plain-English summary
Spineart SA is recalling 8 units of the Tryptik 2 C-Plate Self Tapping Polyaxial Screw, 4.5 mm, length 18 mm, reference TRY-PS-45 18-S. The recall is limited to units with batch number 3-5939 that were distributed in California.
The recall was initiated because the product labeling for the Tryptik 2-C-Plate Self Tapping screw, reference TRY-PS 40, Lot 3-5934, contains a sketch or drawing of a self-drilling screw. This labeling error does not match the specific product being recalled.
The Tryptik 2C-Plate Anterior Cervical Plate System is intended for temporary stabilization of the cervical spine (C2-C7) during spinal fusion. Healthcare providers and patients who have received these specific units should contact Spineart SA for further instructions.
The recalled product
- Product
- TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.5 MM, LENGTH 18 MM, REF TRY-PS-45 18-S, Qty 2 TRYPTIK(R) 2C-Plate Anterior Cervical Plate System is intended to be used for temporary stabilization of the cervical spine (C2-C7) during the development of solid spinal fusion…
- Manufacturer
- SPINEART SA
- Hazard
- Affected units
- 8
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- batch: 3-5939
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 7 recalled by SPINEART SA under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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