Bausch & Lomb, Inc. recalls

11 recalls in our records from 2012 to 2024: 6 FDA drugs, 4 FDA medical devices, 1 CPSC.

Recalls with full detail pages

• CPSC · Consumer productMay 2, 2024

  Bausch + Lomb Recalls Project Watson Eyelid Wipes for Dogs Due to Risk of Exposure to Bacteria and Fungi

  When the recalled dog eyelid wipes are opened and in use, bacteria and fungi, which are organisms found widely in the environment, soil, and water, can be introduced and…

Earlier and other recalls

These link to the official agency notice.

• FDA · DrugsClass IIIJun 19, 2019

  Bausch & Lomb drug recall: Lotemax Official notice ↗

  Failed Stability Specifications: Out of specification for viscosity.

• FDA · Medical devicesClass IIOct 3, 2018

  Bausch & Lomb Inc medical device recall: Bausch + Lomb Stellaris Elite 20 GA Vit Cutter Official notice ↗

  The back cap separates from the body of the vitrectomy cutter.

• FDA · DrugsClass IIJun 21, 2017

  Bausch & Lomb, Inc. drug recall: NasalCrom Official notice ↗

  CGMP Deviations: Possibility of the presence of microbial contamination in the water used to manufacture this product lot.

• FDA · Medical devicesClass IIJan 18, 2017

  Bausch & Lomb, Inc. medical device recall: Algerbrush-II Product Usage: Medical - For surgeons to use in… Official notice ↗

  According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging operator notified his supervisor he had not placed the operating instruction into the last…

• FDA · DrugsClass IIIFeb 3, 2016

  Bausch & Lomb, Inc. drug recall: Cyclopentolate Hydrochloride Ophthalmic Solution USP Official notice ↗

  Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.

• FDA · DrugsClass IIAug 26, 2015

  Bausch & Lomb, Inc. drug recall: Bromfenac Ophthalmic Solution Official notice ↗

  Lack of Assurance of Sterility: Failed preservative effectiveness testing.

• FDA · Medical devicesClass IIDec 31, 2014

  Bausch & Lomb Inc medical device recall: Bausch & Lomb Stellaris PC w/ Laser Official notice ↗

  A software anomaly was identified where the system may automatically transition from "Standby" to "Ready to Fire" state while in surgical use.

• FDA · DrugsClass IIJul 2, 2014

  Bausch & Lomb, Inc. drug recall: Muro 128 Official notice ↗

  Crystallization: Crystal precipitate formation and an increase in the number of complaints associated with a gritty, sand-like feeling in the eye.

• FDA · Medical devicesClass IIDec 26, 2012

  Bausch & Lomb Inc medical device recall: Bausch + Lomb Stellaris PC Vision Enhancement System Official notice ↗

  Posterior fluidics modules installed in the system may need to be recalibrated.

• FDA · DrugsClass IIJun 20, 2012

  Bausch & Lomb, Inc. drug recall: Murocel Official notice ↗

  Lack of Assurance of Sterility: Bausch & Lomb, Inc. is recalling 7 Lots of Murocel Methylcellulose Lubricant Opthalmic Solution 1% (15 mL). Product was found to be OOS…

Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.