CTL Medical Recalls CEZANNE II TLIF Bullet-Tip Cage Due to Fracture Reports
CTL Medical Corporation is recalling 39 units of CEZANNE II TLIF Bullet-Tip Cages because reports indicate the devices fractured during insertion.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, and the source text reports that the device fractured during insertion, which constitutes a significant injury risk for a medical device.
Plain-English summary
CTL Medical Corporation is recalling 39 units of the CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H7mm, Part #018.1907. The recall is being conducted because reports were received indicating that the device fractured during insertion.
The affected units are identified by lot numbers 14LEDODB, 15CNDOGC, and 15DJDOEC. Distribution of these devices was made to Arizona, Florida, Indiana, Kansas, Massachusetts, Michigan, New York, Tennessee, and Texas.
Healthcare providers and patients should contact CTL Medical Corporation for further information regarding the recall and potential replacement or repair options.
The recalled product
- Product
- CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H7mm, Part #018.1907.
- Manufacturer
- CTL Medical Corporation
- Category
- Medical Device — Spinal Implant
- Hazard
- Affected units
- 39
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 (3)
- Lot numbers 14LEDODB
- 15CNDOGC
- and 15DJDOEC .
Distribution
Part of a larger recall action
This product is one of 4 recalled by CTL Medical Corporation 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.
See all 4 products in this recall →Related recalls
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