Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 15, 2014
MaxLock Extreme Mod-Foot Concave Reamer; Individually packaged in a 3 x 4 bag and heat sealed with label on the outside. Used during procedures to clear away bone and cartilage within the desired implant area.
Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot Concave Reamer
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Orthohelix Surgical Designs Inc recalled MaxLock Extreme Mod-Foot Concave Reamer; Individually packaged in a 3 x 4 bag and heat se… - a moderate-severity action.
MaxLock Extreme Mod-Foot Concave Reamer; Individually packaged in a 3 x 4 bag and heat se… was recalled by Orthohelix Surgical Designs Inc in October 15, 2014. Reason: Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot Concave Reamer. Check the official notice for the remedy. Verify recall #Z-0062-2015 with the FDA Devices before acting.
The recall
Orthohelix Surgical Designs Inc issued this moderate-severity FDA Devices recall-Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot Concave Reamer.
- Moderate
- severity level
- 38 units
- affected scope
- Class II
- classification
- October 15, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0062-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0062-2015) was formally reported on October 15, 2014, with the manufacturer initiating the action on September 19, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Orthohelix Surgical Designs Inc is listed as the recalling firm, operating out of Medina, OH. Federal records list the affected scope as 38.
The documented reason for this recall is: Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot Concave Reamer Distribution data in the federal record shows the product reached: USA Distribution -- in the states of WI, NM, TX, WA, MO, OH, UT, TN, MI, VA, NC, VA, and PA.. 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
38
Related Recalls
6
3 from same agency
Product description
MaxLock Extreme Mod-Foot Concave Reamer; Individually packaged in a 3 x 4 bag and heat sealed with label on the outside. Used during procedures to clear away bone and cartilage within the desired implant area.
Reason for recall
Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot Concave Reamer
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0062-2015 |
| Date reported | October 15, 2014 |
| Date initiated | September 19, 2014 |
| Recalling firm | Orthohelix Surgical Designs Inc |
| Firm location | Medina, OH |
| Affected scope | 38 |
| Distribution | USA Distribution -- in the states of WI, NM, TX, WA, MO, OH, UT, TN, MI, VA, NC, VA, and PA. |
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-0062-2015) 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? ▼
MaxLock Extreme Mod-Foot Concave Reamer; Individually packaged in a 3 x 4 bag and heat sealed with label on the outside. Used during procedures to clear away bone and cartilage within the desired implant area.. Recalled by Orthohelix Surgical Designs Inc. Units affected: 38.
Why was this product recalled? ▼
Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot Concave Reamer
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 15, 2014. Severity: Moderate. Recall number: Z-0062-2015.
Where was the recalled product distributed? ▼
Distribution: USA Distribution -- in the states of WI, NM, TX, WA, MO, OH, UT, TN, MI, VA, NC, VA, and PA..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0062-2015) 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 October 15, 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.