PlainRecalls

Richard Wolf GmbH

10 recalls on record · Latest: May 21, 2025

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Agency notice ledger

Federal filing book Richard Wolf GmbH LIGHT-BOOK · SINGLE-AGENCY

#1,513 of 14,151 · 10 notices · 0.010% archive

  • BOOK 10 notices
  • RANK #1,513 of 14,151
  • SHARE 0.010% archive
  • AGENCY FDA Devices (10)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 21, 2025
  • PHOTO 4 Earth Farms formerl…

Nearest notice-volume peer: 4 Earth Farms formerly Mcl Fresh Inc (0 notice gap)

Richard Wolf GmbH accounts for about 0.010% of the 104,423-notice archive on 10 distinct filings — a mid 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 Richard Wolf GmbH compares to 14,151 recalling firms

Richard Wolf GmbH ranks 1,513th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Richard Wolf GmbH vs all firms by recall-notice count

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

10 1513th of 14151 higher than 12,602 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

Richard Wolf GmbH in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Richard Wolf GmbH holds about 0.010% of archive notices alongside 10 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate May 21, 2025

PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).

FDA Devices Moderate May 3, 2023

FLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.051

FDA Devices Moderate May 3, 2023

FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 828.051

FDA Devices Moderate May 3, 2023

FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685

FDA Devices Moderate May 3, 2023

FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.685

FDA Devices Moderate Aug 18, 2021

CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323

FDA Devices Moderate Aug 5, 2020

Tube Set for TEM - Product Usage: Transanal Endoscopic Microsurgery (TEM) combination system and the instrument set for the TEM procedure are designed to provide access to the rectal cavity and accessible part of the lower sigmoid colon using a stereo and/or monocular endoscope under gas tight conditions for the excision of polyps and/or the removal of tumors that have been previously staged.

FDA Devices Moderate Feb 13, 2019

Richard Wolf Bronchoscope Tubes, Model Texas. Device is reusable and should be sterilized prior to each use. Product Usage: Bronchoscopes are intended for investigation, diagnosis and therapy of pathological changes and removal of foreign bodies in the area of the tracheobronchial respiratory pathways, in conjunction with endoscopic accessories. The bronchoscopes can also be used endoscopically to visualize the tracheobionchial respiratory tract via the natural passage (oral). Tracheoscope tube

FDA Devices Moderate Aug 29, 2018

Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically created passages. Product Usage: Device is a standard punch; standard punches are used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically created passages.

FDA Devices Moderate May 23, 2018

RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery.

Richard Wolf GmbH holds a measurable archive slice

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 Richard Wolf GmbH?
PlainRecalls indexes 10 distinct federal recall events naming Richard Wolf GmbH, 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 Richard Wolf GmbH sit among other recalling firms?
Richard Wolf GmbH ranks #1,513 of 14,151 by distinct recall-event count among 14,151 firms in this archive (89th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Richard Wolf GmbH's notices?
FDA Devices accounts for 10 of this firm's 10 indexed notices.
What product category dominates Richard Wolf GmbH's filing book?
Filings for Richard Wolf GmbH 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.
Richard Wolf GmbH: 10 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 Richard Wolf GmbH; individual notices remain authoritative on each linked recall page.

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