ModerateClass IITerminated

FDA Devices recall · Reported August 12, 2015

Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton TCS Interbody Fusion Device, spinal implant. Part Numbers / Product Description: 5302-3514 / 03.5 x 14mm Locking Screws; 5302-3516 / 03.5 x 16mm Locking Screws; 502-3518 / 03.5 x 18mm Locking Screws; 5302-3814 / 03.8 x 14mm Locking Screws; 5302-3816 / 03.8 x 16 mm Locking Screws; 5302-3818 / 03.8 x 18mm Locking Screws.

Q: Which agency issued this recall?

This recall was issued by the FDA Devices on August 12, 2015. Severity: Moderate. Recall number: Z-2327-2015.

Q: Where was the recalled product distributed?

Distribution: Distributed in the states of CA, TX, OK, MA, NY, IN, OR, and GA..

Q: How do I check if my product is affected by a recall?

Check the product description and recall number (Z-2327-2015) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.

Q: Should I stop using a recalled medication or medical device?

Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking bone screw collars not 'locking'.

Recall #: Z-2327-2015
Affected scope: 137 units
Initiated: July 20, 2015

Compiled from official public sources by the editorial team. · Updated July 2026

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Titan Spine, LLC recalled Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton T… - a moderate-severity action.

Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton T… was recalled by Titan Spine, LLC in August 12, 2015. Reason: Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking …. Check the official notice for the remedy. Verify recall #Z-2327-2015 with the FDA Devices before acting.

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The recall

Titan Spine, LLC issued this moderate-severity FDA Devices recall-Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking ….

Moderate
severity level: 137 units
affected scope: Class II
classification: August 12, 2015
reported

Sourced from official FDA Devices enforcement records. Verify recall #Z-2327-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Devices action (record #Z-2327-2015) was formally reported on August 12, 2015, with the manufacturer initiating the action on July 20, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Titan Spine, LLC is listed as the recalling firm, operating out of Mequon, WI. Federal records list the affected scope as 137 units.

The documented reason for this recall is: Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking bone screw collars not 'locking'. Distribution data in the federal record shows the product reached: Distributed in the states of CA, TX, OK, MA, NY, IN, OR, and GA.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Moderate

Affected scope

137 units

Related Recalls

3 from same agency

Product description

Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton TCS Interbody Fusion Device, spinal implant. Part Numbers / Product Description: 5302-3514 / 03.5 x 14mm Locking Screws; 5302-3516 / 03.5 x 16mm Locking Screws; 502-3518 / 03.5 x 18mm Locking Screws; 5302-3814 / 03.8 x 14mm Locking Screws; 5302-3816 / 03.8 x 16 mm Locking Screws; 5302-3818 / 03.8 x 18mm Locking Screws.

Reason for recall

Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking bone screw collars not 'locking'.

Recall Profile

Structured summary of the FDA Devices recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Moderate (Class II)
Status	Terminated
Recall number	Z-2327-2015
Date reported	August 12, 2015
Date initiated	July 20, 2015
Recalling firm	Titan Spine, LLC
Firm location	Mequon, WI
Affected scope	137 units
Distribution	Distributed in the states of CA, TX, OK, MA, NY, IN, OR, and GA.

Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

137 units units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall

Multi-state (10K – 100K units) -

Large-scale (100K – 1M units) -

Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (Z-2327-2015) and product description against the item you own. Search the archive
Confirm the current status with FDA Devices before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

Why was this product recalled? ▼

Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking bone screw collars not 'locking'.

Which agency issued this recall? ▼

This recall was issued by the FDA Devices on August 12, 2015. Severity: Moderate. Recall number: Z-2327-2015.

Where was the recalled product distributed? ▼

Distribution: Distributed in the states of CA, TX, OK, MA, NY, IN, OR, and GA..

How do I check if my product is affected by a recall? ▼

Check the product description and recall number (Z-2327-2015) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.

Should I stop using a recalled medication or medical device? ▼

Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported August 12, 2015. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.