Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported September 25, 2013
Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M. To augment or reconstruct underdeveloped or traumatized mandibular region.
Implantech initiated a voluntary recall of certain lots of Terino Square Chin-Style II-Medicum (Lot # 848488 and 850156), after determining that the devices from the lot numbers d…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Implantech Associates Inc recalled Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M. To augment o… - a moderate-severity action.
Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M. To augment o… was recalled by Implantech Associates Inc in September 25, 2013. Reason: Implantech initiated a voluntary recall of certain lots of Terino Square Chin-Style II-Medicum (Lot # 848488 …. Check the official notice for the remedy. Verify recall #Z-2211-2013 with the FDA Devices before acting.
The recall
Implantech Associates Inc issued this moderate-severity FDA Devices recall-Implantech initiated a voluntary recall of certain lots of Terino Square Chin-Style II-Medicum (Lot # 848488 ….
- Moderate
- severity level
- 8 units
- affected scope
- Class II
- classification
- September 25, 2013
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2211-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2211-2013) was formally reported on September 25, 2013, with the manufacturer initiating the action on August 30, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Implantech Associates Inc is listed as the recalling firm, operating out of Ventura, CA. Federal records list the affected scope as 8.
The documented reason for this recall is: Implantech initiated a voluntary recall of certain lots of Terino Square Chin-Style II-Medicum (Lot # 848488 and 850156), after determining that the devices from the lot numbers do not conform to the dimensional require… Distribution data in the federal record shows the product reached: Worldwide distribution: US (nationwide) including states of NY, KY, and CO, and the country of Israel.. 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
8
Related Recalls
6
3 from same agency
Product description
Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M. To augment or reconstruct underdeveloped or traumatized mandibular region.
Reason for recall
Implantech initiated a voluntary recall of certain lots of Terino Square Chin-Style II-Medicum (Lot # 848488 and 850156), after determining that the devices from the lot numbers do not conform to the dimensional requirements for the TSCII-M.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2211-2013 |
| Date reported | September 25, 2013 |
| Date initiated | August 30, 2013 |
| Recalling firm | Implantech Associates Inc |
| Firm location | Ventura, CA |
| Affected scope | 8 |
| Distribution | Worldwide distribution: US (nationwide) including states of NY, KY, and CO, and the country of Israel. |
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-2211-2013) 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? ▼
Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M. To augment or reconstruct underdeveloped or traumatized mandibular region.. Recalled by Implantech Associates Inc. Units affected: 8.
Why was this product recalled? ▼
Implantech initiated a voluntary recall of certain lots of Terino Square Chin-Style II-Medicum (Lot # 848488 and 850156), after determining that the devices from the lot numbers do not conform to the dimensional requirements for the TSCII-M.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 25, 2013. Severity: Moderate. Recall number: Z-2211-2013.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution: US (nationwide) including states of NY, KY, and CO, and the country of Israel..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2211-2013) 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 September 25, 2013. 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.