PlainRecalls

Resmed Corporation

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Aug 24, 2016

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Agency notice ledger

Federal filing book Resmed Corporation LIGHT-BOOK · SINGLE-AGENCY

#5,654 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,654 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 24, 2016
  • PHOTO 3M Company

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

Resmed Corporation 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 →

Resmed Corporation's standing among 14,151 recalling firms

Resmed Corporation ranks 5,654th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Resmed Corporation vs all firms by recall-notice count

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

2 5654th 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 · 2026-09-15

Resmed Corporation in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Resmed Corporation 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 Aug 24, 2016

Quattro Air FFM MED  AMER, Product Code: 62702, full face mask for use with active-exhaust-valve ventilators
FDA Devices Moderate Feb 10, 2016

Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for example, the largest population of patients on the Astral device is COPD patients primarily using the device at night with some daytime use for recovery breathing. While it is possible that there may be scenarios where critically dependent patients may encounter this scenario, the likelihood of this leading to harm is negligible because critically dependent patients will have

Resmed Corporation 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 Resmed Corporation? ▼
PlainRecalls indexes 2 distinct federal recall events naming Resmed Corporation, 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 Resmed Corporation sit among other recalling firms? ▼
Resmed Corporation ranks #5,654 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 Resmed Corporation's notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Resmed Corporation's filing book? ▼
Filings for Resmed Corporation 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.
Resmed Corporation: 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 Resmed Corporation; individual notices remain authoritative on each linked recall page.

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