PlainRecalls

The Metrix Company

Compiled from official public sources by the publisher.

33 recalls on record · Latest: Nov 20, 2024

Subscribe to new The Metrix Company recalls (RSS)

Agency notice ledger

Federal filing book The Metrix Company MID-BOOK · SINGLE-AGENCY

#516 of 14,151 · 33 notices · 0.032% archive

  • BOOK 33 notices
  • RANK #516 of 14,151
  • SHARE 0.032% archive
  • AGENCY FDA Devices (33)
  • CAT medical devices
  • CATS 1 category
  • LATEST Nov 20, 2024
  • PHOTO Avkare Inc.

Nearest notice-volume peer: Avkare Inc. (0 notice gap)

The Metrix Company accounts for about 0.032% of the 104,423-notice archive on 33 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 →

How The Metrix Company compares to 14,151 recalling firms

The Metrix Company ranks 516th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

The Metrix Company vs all firms by recall-notice count

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

33 516th of 14151 higher than 13,632 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

The Metrix Company in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows The Metrix Company holds about 0.032% of archive notices alongside 33 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 20, 2024

SECURE 250 mL EMPTY EVA CONTAINER With 2 Ports, REF 66045; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

SECURE 100 mL EMPTY EVA CONTAINER With 2 Ports, REF 66040; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

Imed Products Imed EVA BAG, 500 mL, 2-PORTS, REF IM68050; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

VYGON 100 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9601; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

Imed Products Imed EVA BAG, 150 mL, 2-PORTS, REF IM38040; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

CORMIX 150 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64040; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

SECURE 50 mL EMPTY EVA CONTAINER With 2 Ports, REF 66042; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

Imed Products Imed EVA BAG, 250 mL, 2-PORTS, REF IM68045; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

CORMIX 500 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64050; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

CORMIX 250 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64045; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

SECURE 100 mL EMPTY EVA CONTAINER With 2 Ports (Bulk Packed), REF 66041; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

SECURE 50 mL EMPTY EVA CONTAINER With 2 Ports (Bulk Packed) , REF 66043; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

VYGON 250 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9602; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

SECURE 500 mL EMPTY EVA CONTAINER With 2 Ports, REF 66050; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

Imed Products Imed EVA BAG, 1000 mL, 2-PORTS, REF IM68055; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Nov 20, 2024

SECURE 1000 mL EMPTY EVA CONTAINER With 2 Ports, REF 66055; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
FDA Devices Moderate Oct 9, 2019

SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 4000mL, (legless) REF 66640 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
FDA Devices Moderate Oct 9, 2019

SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 1500mL, REF 66616 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
FDA Devices Moderate Oct 9, 2019

SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 3000mL, REF 66631 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
FDA Devices Moderate Oct 9, 2019

ExactaMix, Model: H938905, EMPTY EVA DUAL CHAMBER CONTAINER With Screw Connectors, 250 ml/ 1250 ml, Baxter - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
FDA Devices Moderate Oct 9, 2019

SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 1500mL, (legless) REF 66615 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
FDA Devices Moderate Oct 9, 2019

ExactaMix, Model: H938901, EMPTY EVA DUAL CHAMBER CONTAINER With Screw Connectors, 500 ml/ 2500 ml, Baxter - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
FDA Devices Moderate Oct 9, 2019

SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 4000mL, REF 66641 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
FDA Devices Moderate Oct 9, 2019

SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 3000mL, (legless) REF 66630 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
FDA Devices Moderate Oct 11, 2017

SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40), REF 58719, STERILE R,
FDA Devices Moderate Aug 3, 2016

AUTOCOMP6 XPS High Speed Compounder REF 58810
FDA Devices Moderate Aug 3, 2016

AUTOCOMP6 High Speed Compounder
FDA Devices Moderate Aug 3, 2016

AUTOCOMP6 XP High Speed Compounder REF 58810
FDA Devices Moderate Aug 3, 2016

Container fill and transfer sets, automatic fill compatible, 250 mL, 500 mL, 1000 mL, 1500 mL, 2000 mL, 3000 mL, or 4000 mL.
FDA Devices Moderate Aug 3, 2016

Container fill and transfer sets, 250 mL, 500 mL, 1000 mL, 2000 mL, 3000 mL, or 4000 mL.
FDA Devices Moderate Aug 3, 2016

Dual Chamber Container fill with gravity/attached transfer sets, 250 mL / 1250 mL, 300 mL / 1700 mL, 500 mL / 2500 mL, 500 mL / 3500 mL
FDA Devices Moderate Aug 3, 2016

Container fill and transfer sets, 250 mL and 500 mL, . .
FDA Devices Moderate Aug 3, 2016

Dual Chamber Container fill and transfer sets, 250 mL / 1250 mL or 500 mL / 2500 mL

The Metrix Company holds a measurable archive slice

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.

CooperVision, Inc. 33 Custom Healthcare Systems, Inc. 33 Implant Direct Sybron Manufacturing LLC 33 Inpeco S.a. 33

Frequently Asked Questions

How many federal recall notices name The Metrix Company? ▼
PlainRecalls indexes 33 distinct federal recall events naming The Metrix Company, 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 The Metrix Company sit among other recalling firms? ▼
The Metrix Company ranks #516 of 14,151 by distinct recall-event count among 14,151 firms in this archive (96th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of The Metrix Company's notices? ▼
FDA Devices accounts for 33 of this firm's 33 indexed notices.
What product category dominates The Metrix Company's filing book? ▼
Filings for The Metrix Company 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.
The Metrix Company: 33 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 The Metrix Company; individual notices remain authoritative on each linked recall page.

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