PlainRecalls

Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Compiled from official public sources by the publisher.

4 recalls on record · Latest: May 6, 2020

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Agency notice ledger

Federal filing book Kerr/Pentron, DBA Kerr Corp… LIGHT-BOOK · SINGLE-AGENCY

#2,994 of 14,151 · 4 notices · 0.004% archive

  • BOOK 4 notices
  • RANK #2,994 of 14,151
  • SHARE 0.004% archive
  • AGENCY FDA Devices (4)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 6, 2020
  • PHOTO 1 Epic, LLC

Nearest notice-volume peer: 1 Epic, LLC (0 notice gap)

Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical accounts for about 0.004% of the 104,423-notice archive on 4 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Kerr/Pentron, DBA Kerr Corp… compares to 14,151 recalling firms

Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical ranks 2,994th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Kerr/Pentron, DBA Kerr Corp… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

4 2994th of 14151 higher than 10,859 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-15

Kerr/Pentron, DBA Kerr Corp… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical holds about 0.004% of archive notices alongside 4 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate May 6, 2020

Nexus Universal with OptiBond Universal, Universal Adhesive Resin Cement, Trial Kit, Ref # 36990 - Product Usage: The intended use of this device is to be used for the cementation of indirect restorations including veneers, inlays, onlays, bridges, posts, and the cementation of crown restorations to implant abutments.
FDA Devices Moderate Jun 12, 2019

Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution
FDA Devices Moderate Sep 25, 2013

NX3 Try-In Gel. The product is used as a tooth shade resin material.
FDA Devices Moderate Apr 17, 2013

Kerr Maxcem Elite, self-etch/self-adhesive resin cement; Intro Kit Part No. 34417; DMC 0446 Rev 0. Used for cementation of all indirect restorations.

Kerr/Pentron, DBA Kerr Corp… is a small archive contributor

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (4 here).

1 Epic, LLC 4 3rd Day Beverages LLC 4 A.p. Deauville, LLC 4 Aaa Pharmaceutical, Inc. 4 Aap Implantate Ag 4

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Aap Implantate Ag 4 Ab Sciex, LLC 4 Accelerate Diagnostics Inc 4 Accord Media, LLC 4

Frequently Asked Questions

How many federal recall notices name Kerr/Pentron, DBA Kerr Corp…? ▼
PlainRecalls indexes 4 distinct federal recall events naming Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Kerr/Pentron, DBA Kerr Corp… sit among other recalling firms? ▼
Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical ranks #2,994 of 14,151 by distinct recall-event count among 14,151 firms in this archive (77th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Kerr/Pentron, DBA Kerr Corp…'s notices? ▼
FDA Devices accounts for 4 of this firm's 4 indexed notices.
What product category dominates Kerr/Pentron, DBA Kerr Corp…'s filing book? ▼
Filings for Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical: 4 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026