PlainRecalls
ModerateClass IITerminated

FDA Devices recall · Reported April 25, 2018

Stage-1 Tissue Punch, Disposable, 4.5mm; catalog number: ISS141K. Intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations.

The cutting edge of tissue punches may be potentially damaged with small dents and nicks.

Recall #
Z-1443-2018
Affected scope
101
Initiated
January 24, 2018
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Keystone Dental Inc recalled Stage-1 Tissue Punch, Disposable, 4.5mm; catalog number: ISS141K. Intended for use in … - a moderate-severity action.

Stage-1 Tissue Punch, Disposable, 4.5mm; catalog number: ISS141K. Intended for use in … was recalled by Keystone Dental Inc in April 25, 2018. Reason: The cutting edge of tissue punches may be potentially damaged with small dents and nicks.. Check the official notice for the remedy. Verify recall #Z-1443-2018 with the FDA Devices before acting.

The recall

Keystone Dental Inc issued this moderate-severity FDA Devices recall-The cutting edge of tissue punches may be potentially damaged with small dents and nicks..

Moderate
severity level
101 units
affected scope
Class II
classification
April 25, 2018
reported

Sourced from official FDA Devices enforcement records. Verify recall #Z-1443-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. 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.

Medical Devices recalls over time

Where this recall sits in its category - 41,021 medical devices recalls on record

01,0002,0003,0004,000 20052008201120142017202020232026 1,947
Severity1906864652High severity (most serious)Moderate severityLow severity
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

Stage-1 Tissue Punch, Disposable, 4.5mm; catalog number: ISS141K. Intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations.

Reason for recall

The cutting edge of tissue punches may be potentially damaged with small dents and nicks.

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-1443-2018
Date reported April 25, 2018
Date initiated January 24, 2018
Recalling firm Keystone Dental Inc
Firm location Burlington, MA
Affected scope 101
Distribution Worldwide Distribution -- US, to the state of California; and, the countries of Canada and Germany

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

Scale of Impact

101 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-1443-2018) 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? ▼
Stage-1 Tissue Punch, Disposable, 4.5mm; catalog number: ISS141K. Intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations.. Recalled by Keystone Dental Inc. Units affected: 101.
Why was this product recalled? ▼
The cutting edge of tissue punches may be potentially damaged with small dents and nicks.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 25, 2018. Severity: Moderate. Recall number: Z-1443-2018.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution -- US, to the state of California; and, the countries of Canada and Germany.
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

Drug and device notices outside this firm and state, matched by severity timing and product category.

Compare this recall with GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VS… → · All Medical Devices recalls

This recall: FDA Devices, reported April 25, 2018. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026