PlainRecalls

Aap Implantate Ag

Compiled from official public sources by the publisher.

4 recalls on record · Latest: Apr 15, 2020

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Agency notice ledger

Federal filing book Aap Implantate Ag LIGHT-BOOK · SINGLE-AGENCY

#2,745 of 14,151 · 4 notices · 0.004% archive

  • BOOK 4 notices
  • RANK #2,745 of 14,151
  • SHARE 0.004% archive
  • AGENCY FDA Devices (4)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 15, 2020
  • PHOTO 1 Epic, LLC

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

Aap Implantate Ag 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 →

Aap Implantate Ag's standing among 14,151 recalling firms

Aap Implantate Ag ranks 2,745th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Aap Implantate Ag vs all firms by recall-notice count

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

4 2745th 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 · 2026-09-16

Aap Implantate Ag in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Aap Implantate Ag 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 Apr 15, 2020

aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00
FDA Devices Low Jan 1, 2020

INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453
FDA Devices Low Jan 1, 2020

INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425
FDA Devices Moderate Mar 27, 2019

aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended for multiple use.

Aap Implantate Ag 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 Aap Implantate Ag? ▼
PlainRecalls indexes 4 distinct federal recall events naming Aap Implantate Ag, 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 Aap Implantate Ag sit among other recalling firms? ▼
Aap Implantate Ag ranks #2,745 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 Aap Implantate Ag's notices? ▼
FDA Devices accounts for 4 of this firm's 4 indexed notices.
What product category dominates Aap Implantate Ag's filing book? ▼
Filings for Aap Implantate Ag 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.
Aap Implantate Ag: 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 Aap Implantate Ag; individual notices remain authoritative on each linked recall page.

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