PlainRecalls

Epix Therapeutics, INC

Compiled from official public sources by the publisher.

6 recalls on record · Latest: Apr 7, 2021

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Agency notice ledger

Federal filing book Epix Therapeutics, INC LIGHT-BOOK · SINGLE-AGENCY

#2,148 of 14,151 · 6 notices · 0.006% archive

  • BOOK 6 notices
  • RANK #2,148 of 14,151
  • SHARE 0.006% archive
  • AGENCY FDA Devices (6)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 7, 2021
  • PHOTO 1908 Brands

Nearest notice-volume peer: 1908 Brands (0 notice gap)

Epix Therapeutics, INC accounts for about 0.006% of the 104,423-notice archive on 6 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Epix Therapeutics, INC sits among 14,151 recalling firms

Epix Therapeutics, INC ranks 2,148th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Epix Therapeutics, INC vs all firms by recall-notice count

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

6 2148th of 14151 higher than 11,804 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 · 2026-09-27

Epix Therapeutics, INC in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Epix Therapeutics, INC holds about 0.006% of archive notices alongside 6 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Apr 7, 2021

EPIX Therapeutics DiamondTemp Bidrectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:CEDTB400L, SterileEO, UDI: 00812499030303
FDA Devices Moderate Apr 7, 2021

EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Small Curve, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:DT100S,SterileEO, Rx Only, UDI: 00812499030006
FDA Devices Moderate Apr 7, 2021

EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Large Curve, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:DT200L, SterileEO, Rx Only, UDI: 00812499030013
FDA Devices Moderate Apr 7, 2021

EPIX Therapeutics DiamondTemp Bidrectional Small Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:CEDTB300S, SterileEO, UDI: 00812499030358
FDA Devices Moderate Apr 7, 2021

EPIX Therapeutics DiamondTemp Unidirectional Small Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF CEDT100S, SterileEO, UDI 00812499030198
FDA Devices Moderate Apr 7, 2021

EPIX Therapeutics DiamondTemp Unidirectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF: CEDT200L, Sterile EO, UDI: 00812499030259

Epix Therapeutics, INC holds a measurable archive slice

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 (6 here).

1908 Brands 6 Abbott Molecular 6 Advance Medical Designs, Inc. 6 Air Stream Corp. 6 Aire-Master of America Inc 6

Similar medical devices volume

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

Abbott Molecular 6 Advance Medical Designs, Inc. 6 American Medical Systems, Inc. 6 Animas Corporation 6

Frequently Asked Questions

How many federal recall notices name Epix Therapeutics, INC? ▼
PlainRecalls indexes 6 distinct federal recall events naming Epix Therapeutics, 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 Epix Therapeutics, INC sit among other recalling firms? ▼
Epix Therapeutics, INC ranks #2,148 of 14,151 by distinct recall-event count among 14,151 firms in this archive (83rd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Epix Therapeutics, INC's notices? ▼
FDA Devices accounts for 6 of this firm's 6 indexed notices.
What product category dominates Epix Therapeutics, INC's filing book? ▼
Filings for Epix Therapeutics, 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.
Epix Therapeutics, INC: 6 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 Epix Therapeutics, INC; individual notices remain authoritative on each linked recall page.

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