Phantom TTC Nail, 10.0 X 200mm, Right

Medical devices distributed, prior to sterilization

Recall #: Z-1254-2024
Initiated: December 21, 2023

Compiled from official public sources by the publisher. · Updated September 2026

Paragon 28, Inc. recalled Phantom TTC Nail, 10.0 X 200mm, Right - a moderate-severity action.

Phantom TTC Nail, 10.0 X 200mm, Right was recalled by Paragon 28, Inc. in March 13, 2024. Reason: Medical devices distributed, prior to sterilization. Check the official notice for the remedy. Verify recall #Z-1254-2024 with the FDA Devices before acting.

The recall

Paragon 28, Inc. issued this moderate-severity FDA Devices recall-Medical devices distributed, prior to sterilization.

Moderate
severity level: Class II
classification: March 13, 2024
reported

Sourced from official FDA Devices enforcement records. Verify recall #Z-1254-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

The number of affected units is not disclosed in the agency filing, which is common for drug and food recalls where lot-level tracking supersedes unit counts. Distribution scope (see Distribution below) 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, 6 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 agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.

Product description

Phantom TTC Nail, 10.0 X 200mm, Right

Reason for recall

Medical devices distributed, prior to sterilization

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	Ongoing
Recall number	Z-1254-2024
Date reported	March 13, 2024
Date initiated	December 21, 2023
Recalling firm	Paragon 28, Inc.
Firm location	Englewood, CO
Affected scope	Not disclosed
Distribution	US:CA OUS: None

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

What to do with this recall

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

Check the recall number (Z-1254-2024) 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? ▼

Phantom TTC Nail, 10.0 X 200mm, Right. Recalled by Paragon 28, Inc..

Why was this product recalled? ▼

Medical devices distributed, prior to sterilization

Which agency issued this recall? ▼

This recall was issued by the FDA Devices on March 13, 2024. Severity: Moderate. Recall number: Z-1254-2024.

Where was the recalled product distributed? ▼

Distribution: US:CA OUS: None.

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.

Nationwide recalls with similar severity or category timing

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Similar severity · nearest report date

Same archive severity grade (Moderate), closest by report date among other firms and states.

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Same product category, closest by report date among other firms and states (deduped against the severity set).

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This recall: FDA Devices, reported March 13, 2024. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026