Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported April 9, 2014
AOA Distalizer Lock Nut Screw, found in products listed as: Distal Jet, Spring Jet, Mesial Jet, and Uprighter Jet. Removable functional orthodontic appliances that are to modify the growth of the jaws in a prescribed growth pattern.
The Lock Nut component of the Jet appliances may be missing the screw collar, which serves as a mechanical stop to prevent over-tightening in appliance assemby. Without this colla…
Allesee Orthodontic Appliances recalled AOA Distalizer Lock Nut Screw, found in products listed as: Distal Jet, Spring Jet, Mesia… - a moderate-severity action.
AOA Distalizer Lock Nut Screw, found in products listed as: Distal Jet, Spring Jet, Mesia… was recalled by Allesee Orthodontic Appliances in April 9, 2014. Reason: The Lock Nut component of the Jet appliances may be missing the screw collar, which serves as a mechanical st…. Check the official notice for the remedy. Verify recall #Z-1314-2014 with the FDA Devices before acting.
The recall
Allesee Orthodontic Appliances issued this moderate-severity FDA Devices recall-The Lock Nut component of the Jet appliances may be missing the screw collar, which serves as a mechanical st….
- Moderate
- severity level
- 411 units
- affected scope
- Class II
- classification
- April 9, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1314-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1314-2014) was formally reported on April 9, 2014, with the manufacturer initiating the action on February 24, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Allesee Orthodontic Appliances is listed as the recalling firm, operating out of Sturtevant, WI. Federal records list the affected scope as 411.
The documented reason for this recall is: The Lock Nut component of the Jet appliances may be missing the screw collar, which serves as a mechanical stop to prevent over-tightening in appliance assemby. Without this collar, an over-tightened lock nut may stop t… Distribution data in the federal record shows the product reached: Worldwide Distribution: US (nationwide) and the country of : Canada.. 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.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
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.
Affected scope
411
Related Recalls
6
3 from same agency
Product description
AOA Distalizer Lock Nut Screw, found in products listed as: Distal Jet, Spring Jet, Mesial Jet, and Uprighter Jet. Removable functional orthodontic appliances that are to modify the growth of the jaws in a prescribed growth pattern.
Reason for recall
The Lock Nut component of the Jet appliances may be missing the screw collar, which serves as a mechanical stop to prevent over-tightening in appliance assemby. Without this collar, an over-tightened lock nut may stop the piston assembly from moving freely, subsequently preventing intended movement of the teeth.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1314-2014 |
| Date reported | April 9, 2014 |
| Date initiated | February 24, 2014 |
| Recalling firm | Allesee Orthodontic Appliances |
| Firm location | Sturtevant, WI |
| Affected scope | 411 |
| Distribution | Worldwide Distribution: US (nationwide) and the country of : Canada. |
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-1314-2014) 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? ▼
AOA Distalizer Lock Nut Screw, found in products listed as: Distal Jet, Spring Jet, Mesial Jet, and Uprighter Jet. Removable functional orthodontic appliances that are to modify the growth of the jaws in a prescribed growth pattern.. Recalled by Allesee Orthodontic Appliances. Units affected: 411.
Why was this product recalled? ▼
The Lock Nut component of the Jet appliances may be missing the screw collar, which serves as a mechanical stop to prevent over-tightening in appliance assemby. Without this collar, an over-tightened lock nut may stop the piston assembly from moving freely, subsequently preventing intended movement of the teeth.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 9, 2014. Severity: Moderate. Recall number: Z-1314-2014.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution: US (nationwide) and the country of : Canada..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1314-2014) 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 April 9, 2014. 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.