PlainRecalls

Bausch & Lomb Surgical, Inc.

Compiled from official public sources by the publisher.

10 recalls on record · Latest: Sep 3, 2025

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Agency notice ledger

Federal filing book Bausch & Lomb Surgical, Inc. LIGHT-BOOK · SINGLE-AGENCY

#1,426 of 14,151 · 10 notices · 0.010% archive

  • BOOK 10 notices
  • RANK #1,426 of 14,151
  • SHARE 0.010% archive
  • AGENCY FDA Devices (10)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 3, 2025
  • PHOTO 4 Earth Farms formerl…

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

Bausch & Lomb Surgical, Inc. 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 →

Bausch & Lomb Surgical, Inc.'s standing among 14,151 recalling firms

Bausch & Lomb Surgical, Inc. ranks 1,426th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Bausch & Lomb Surgical, Inc. vs all firms by recall-notice count

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

10 1426th 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

Bausch & Lomb Surgical, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Bausch & Lomb Surgical, Inc. 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 Low Sep 3, 2025

Akreos, SKU: AO60P0300. Akreos intraocular lenses
FDA Devices Critical May 14, 2025

Intraocular Lens. enVista Envy IOL, All models starting with EN; enVista Envy Toric IOL, All models starting with ETN.
FDA Devices Critical May 14, 2025

Intraocular lens. enVista Monofocal IOL, All models starting with EE; enVista Aspire IOL, All models starting with EA; enVista Monofocal Toric IOL, All models starting with ETE; enVista Aspire Toric IOL, All models starting with ETA;
FDA Devices Moderate Dec 9, 2020

MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is intended for placement in the capsular bag.
FDA Devices Moderate Jul 22, 2020

enVista one-piece hydrophobic acrylic toric intraocular lens, Bausch and Lomb - Product Usage: is indicated for primary implantation in the capsular bag of the eye in adult patients for visual correction of aphakia and corneal astigmatism following removal of a cataractous lens for improved uncorrected distance vision.
FDA Devices Moderate Dec 26, 2018

enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated for primary implantation for the visual correction of aphakia in adult patients in whom the cataractous lens has been removed. The lens is intended for placement in the capsular bag.
FDA Devices Moderate May 24, 2017

SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or LI61SE 3-piece lens into the eye. The SofPort Easy-Load Lens Delivery System consists of a syringe shaped body and tip with a plunger, drawer, and haptic puller. It is a sterile, disposable plastic device designed for single use only.
FDA Devices Moderate Jul 29, 2015

Bausch & Lomb SoFlex SE Foldable intraocular Lens Product Usage: The SofPort/SoFlex IOLs are intended for primary implantation in the capsular bag of the eye for the visual correction of aphakia secondary to the removal of a cataractous lens in adult patients.
FDA Devices Moderate Jul 29, 2015

Bausch & Lomb SofPort Advanced Optics Aspheric Lens
FDA Devices Moderate Feb 26, 2014

Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos IOL intended for primary implantation in the capsular bag of the eye for the visual correction of aphakia secondary to the removal of a cataractous lens in adult patients.

Bausch & Lomb Surgical, Inc. holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

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

Beekley Corporation 10 Biocare Medical, LLC 10 Carl Zeiss Meditec, Inc. 10 Cypress Medical Products LLC 10

Frequently Asked Questions

How many federal recall notices name Bausch & Lomb Surgical, Inc.? ▼
PlainRecalls indexes 10 distinct federal recall events naming Bausch & Lomb Surgical, Inc., 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 Bausch & Lomb Surgical, Inc. sit among other recalling firms? ▼
Bausch & Lomb Surgical, Inc. ranks #1,426 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 Bausch & Lomb Surgical, Inc.'s notices? ▼
FDA Devices accounts for 10 of this firm's 10 indexed notices.
What product category dominates Bausch & Lomb Surgical, Inc.'s filing book? ▼
Filings for Bausch & Lomb Surgical, Inc. 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.
Bausch & Lomb Surgical, Inc.: 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 Bausch & Lomb Surgical, Inc.; individual notices remain authoritative on each linked recall page.

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