PlainRecalls

Jolife Ab

Compiled from official public sources by the publisher.

2 recalls on record · Latest: May 20, 2026

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Agency notice ledger

Federal filing book Jolife Ab LIGHT-BOOK · SINGLE-AGENCY

#5,114 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,114 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 20, 2026
  • PHOTO 3M Company

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

Jolife Ab 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 →

How Jolife Ab compares to 14,151 recalling firms

Jolife Ab ranks 5,114th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Jolife Ab vs all firms by recall-notice count

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

2 5114th 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 · 2026-09-20

Jolife Ab in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Jolife Ab 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 May 20, 2026

LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog Number: 99576-000043 UDI-DI code: 00883873861875 LUCAS 3.1 Model Number: 99576 Catalog Number: 99576-000063 UDI-DI code: 00883873834329 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss

FDA Devices Moderate Jul 2, 2025

LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.

Jolife Ab 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 Jolife Ab? ▼
PlainRecalls indexes 2 distinct federal recall events naming Jolife Ab, 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 Jolife Ab sit among other recalling firms? ▼
Jolife Ab ranks #5,114 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 Jolife Ab's notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Jolife Ab's filing book? ▼
Filings for Jolife Ab 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.
Jolife Ab: 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 Jolife Ab; individual notices remain authoritative on each linked recall page.

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