PlainRecalls

R82 A/s

Compiled from official public sources by the publisher.

4 recalls on record · Latest: Feb 16, 2022

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Agency notice ledger

Federal filing book R82 A/s LIGHT-BOOK · SINGLE-AGENCY

#3,144 of 14,151 · 4 notices · 0.004% archive

  • BOOK 4 notices
  • RANK #3,144 of 14,151
  • SHARE 0.004% archive
  • AGENCY FDA Devices (4)
  • CAT medical devices
  • CATS 1 category
  • LATEST Feb 16, 2022
  • PHOTO 1 Epic, LLC

Nearest notice-volume peer: 1 Epic, LLC (0 notice gap)

R82 A/s accounts for about 0.004% of the 104,423-notice archive on 4 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 →

R82 A/s's standing among 14,151 recalling firms

R82 A/s ranks 3,144th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

R82 A/s vs all firms by recall-notice count

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

4 3144th of 14151 higher than 10,859 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

R82 A/s in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows R82 A/s holds about 0.004% of archive notices alongside 4 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Feb 16, 2022

R82 by ETAC Push Brace for High-Low
FDA Devices Moderate May 13, 2020

Chest Support for R82 Mustang, Model Numbers: 861810, 861820, 861830; and Rabbit Up, Model Numbers: 869810, 869820, 869830
FDA Devices Moderate May 22, 2019

Wombat Living, Size 3, Item Numbers: 953121-00, 953126-00, 953131-00, 953132-00, 935-135-00, 935136-00, 953211-00, 953221-00, 953222-00, 953225-00, 953226-00, 953231-001, 953232-00, 953236-00 Product Usage: Activity chair (wheelchair)
FDA Devices Moderate Nov 21, 2018

Heron toilet and bath chair Model 880505-01 & 880505-11

R82 A/s is a small archive contributor

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 (4 here).

1 Epic, LLC 4 3rd Day Beverages LLC 4 A.p. Deauville, LLC 4 Aaa Pharmaceutical, Inc. 4 Ab Sciex, LLC 4

Similar medical devices volume

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

Ab Sciex, LLC 4 Accelerate Diagnostics Inc 4 Accord Media, LLC 4 Accumetrics Inc 4

Frequently Asked Questions

How many federal recall notices name R82 A/s? ▼
PlainRecalls indexes 4 distinct federal recall events naming R82 A/s, 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 R82 A/s sit among other recalling firms? ▼
R82 A/s ranks #3,144 of 14,151 by distinct recall-event count among 14,151 firms in this archive (77th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of R82 A/s's notices? ▼
FDA Devices accounts for 4 of this firm's 4 indexed notices.
What product category dominates R82 A/s's filing book? ▼
Filings for R82 A/s 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.
R82 A/s: 4 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 R82 A/s; individual notices remain authoritative on each linked recall page.

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