PlainRecalls

Codman & Shurtleff Inc

59 recalls on record · Latest: Aug 21, 2019

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Agency notice ledger

Federal filing book Codman & Shurtleff Inc MID-BOOK · SINGLE-AGENCY

#300 of 14,151 · 59 notices · 0.057% archive

  • BOOK 59 notices
  • RANK #300 of 14,151
  • SHARE 0.057% archive
  • AGENCY FDA Devices (59)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 21, 2019
  • PHOTO American Health Packa…

Nearest notice-volume peer: American Health Packaging (0 notice gap)

Codman & Shurtleff Inc accounts for about 0.057% of the 104,423-notice archive on 59 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Codman & Shurtleff Inc's standing among 14,151 recalling firms

Codman & Shurtleff Inc ranks 300th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Codman & Shurtleff Inc vs all firms by recall-notice count

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

59 300th of 14151 higher than 13,847 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 · 2026-09-13

Codman & Shurtleff Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Codman & Shurtleff Inc holds about 0.057% of archive notices alongside 59 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Feb 27, 2013

NEUROPATH 6Fx90 GUIDING CATH MPC Product Code: GMC60900000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

FDA Devices Moderate Feb 27, 2013

NEUROPATH 5Fx90 GUIDING CATH ST Product Code: GST50900000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

FDA Devices Moderate Feb 27, 2013

NEUROPATH 6Fx100 GUIDING CATH MPD Product Code: GMD60900000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

FDA Devices Moderate Feb 27, 2013

NEUROPATH 6Fx100 GUIDING CATH MC Product Code: GCB61000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

FDA Devices Moderate Feb 27, 2013

NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GMC51000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

FDA Devices Moderate Feb 27, 2013

NEUROPATH 6Fx100 GUIDING CATH S2 Product Code: GSM61000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

FDA Devices Moderate Feb 27, 2013

NEUROPATH 6Fx100 GUIDING CATH ST Product Code: GST61000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

FDA Devices Moderate Feb 27, 2013

NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

FDA Devices Moderate Feb 27, 2013

NEUROPATH 6Fx90 GUIDING CATH ST Product Code: GST60900000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

Codman & Shurtleff Inc carries an outsized archive share

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

Similar medical devices volume

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

Frequently Asked Questions

How many federal recall notices name Codman & Shurtleff Inc?
PlainRecalls indexes 59 distinct federal recall events naming Codman & Shurtleff Inc, 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 Codman & Shurtleff Inc sit among other recalling firms?
Codman & Shurtleff Inc ranks #300 of 14,151 by distinct recall-event count among 14,151 firms in this archive (98th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Codman & Shurtleff Inc's notices?
FDA Devices accounts for 59 of this firm's 59 indexed notices.
What product category dominates Codman & Shurtleff Inc's filing book?
Filings for Codman & Shurtleff Inc 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.
Codman & Shurtleff Inc: 59 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 Codman & Shurtleff Inc; individual notices remain authoritative on each linked recall page.

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