PlainRecalls

Sendx Medical Inc

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Nov 14, 2012

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Agency notice ledger

Federal filing book Sendx Medical Inc LIGHT-BOOK · SINGLE-AGENCY

#5,728 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,728 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Nov 14, 2012
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Sendx Medical Inc accounts for about 0.002% of the 104,423-notice archive on 2 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 →

Sendx Medical Inc's standing among 14,151 recalling firms

Sendx Medical Inc ranks 5,728th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Sendx Medical Inc vs all firms by recall-notice count

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

2 5728th of 14151 higher than 8,037 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

Sendx Medical Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Sendx Medical Inc holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 14, 2012

ABL80 FLEX CO-OX analyzer, model #393-841 (all software versions prior to 1.35). The ABL80 FLEX CO-OX is a portable, automated analyzer that measures pH, blood gases, electrolytes, glucose and oximetry in whole blood. The ABL80 FLEX CO-OX system is intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point of care setting
FDA Devices Moderate Sep 5, 2012

ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with CO-OX software) - pH Blood Gas and Electrolytes Analyzer System. Intended Use The ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with CO-OX software) are portable, automated analyzers that measure pH, blood gases, electrolytes, glucose and oximetry (ABL80 FLEX CO-OX only) in whole blood. The ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with CO-OX software) analyzer systems are intended for use by trained technologists,

Sendx Medical Inc is a small archive contributor

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

Frequently Asked Questions

How many federal recall notices name Sendx Medical Inc? ▼
PlainRecalls indexes 2 distinct federal recall events naming Sendx Medical 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 Sendx Medical Inc sit among other recalling firms? ▼
Sendx Medical Inc ranks #5,728 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Sendx Medical Inc's notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Sendx Medical Inc's filing book? ▼
Filings for Sendx Medical 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.
Sendx Medical Inc: 2 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 Sendx Medical Inc; individual notices remain authoritative on each linked recall page.

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