PlainRecalls

Procept Biorobotics Corporation

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Sep 1, 2021

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Agency notice ledger

Federal filing book Procept Biorobotics Corpora… LIGHT-BOOK · SINGLE-AGENCY

#5,583 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,583 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 1, 2021
  • PHOTO 3M Company

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

Procept Biorobotics 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 →

How Procept Biorobotics Corpora… compares to 14,151 recalling firms

Procept Biorobotics Corporation ranks 5,583rd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Procept Biorobotics Corpora… vs all firms by recall-notice count

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

2 5583rd 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 · 2026-10-28

Procept Biorobotics Corpora… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Procept Biorobotics Corporation holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of October 2026
FDA Devices Moderate Sep 1, 2021

AQUABEAM Handpiece, REF: HP2000, a sterile single-use component of the AQUABEAM Robotic System.
FDA Devices Moderate Apr 17, 2019

AquaBeam Handpiece, Sterile EO, Rx Only, REF: 310301, and 320301, a component of AquaBeam Robotic System. 320301 distributed outside the U.S. Device Description The AQUABEAM Robotic System is intended for use in patients suffering from lower urinary tract symptoms resulting from benign prostatic hyperplasia (BPH).

Procept Biorobotics Corpora… 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 Procept Biorobotics Corpora…? ▼
PlainRecalls indexes 2 distinct federal recall events naming Procept Biorobotics Corporation, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of October 2026). That count is an issuance inventory, not a hazard score.
Where does Procept Biorobotics Corpora… sit among other recalling firms? ▼
Procept Biorobotics Corporation ranks #5,583 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 Procept Biorobotics Corpora…'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Procept Biorobotics Corpora…'s filing book? ▼
Filings for Procept Biorobotics 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.
Procept Biorobotics 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 Procept Biorobotics Corporation; individual notices remain authoritative on each linked recall page.

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