Bausch & Lomb recalls

Bausch & Lomb has 27 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 19 Jun 2019. The most frequent reason is packaging defects.

Total recalls27since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 19 Jun 2019

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 23 85%Class III 4 15%

Why bausch & lomb is recalled

By year

All bausch & lomb recalls, newest first

27 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIILotemax (loteprednol etabonate ophthalmic gel 0.5%), Sterile recalledLotemaxBausch & LombPotency & AssayNationwide
DeviceCLASS IIBausch + Lomb Stellaris Elite Vision Enhancement System recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vision Enhancement System recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vision Enhancement System recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vit Cutter recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vision Enhancement System recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vision Enhancement System recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vision Enhancement System recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vit Cutter recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vit Cutter recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vision Enhancement System recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vision Enhancement System recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vision Enhancement System recalledBausch & LombPackaging Defects26 states
DeviceCLASS IIBausch + Lomb Stellaris Elite Vision Enhancement System recalledBausch & LombPackaging Defects26 states
DrugCLASS IINasalCrom (cromolyn sodium) Nasal Spray recalled by Bausch & LombBausch & LombSterilityNationwide
DeviceCLASS IIAlgerbrush-II Product Usage: Medical - For surgeons to use recalledBausch & LombPackaging DefectsNationwide
DrugCLASS IIITropicamide Ophthalmic Solution recalled by Bausch & LombTropicamideBausch & LombPackaging DefectsNationwide
DrugCLASS IIITropicamide Ophthalmic Solution recalled by Bausch & LombTropicamideBausch & LombPackaging DefectsNationwide
DrugCLASS IIICyclopentolate Hydrochloride Ophthalmic Solution recalledCyclopentolate HydrochlorideBausch & LombPackaging DefectsNationwide
DrugCLASS IIBromfenac Ophthalmic Solution recalled by Bausch & LombBausch & LombSterilityNationwide
DeviceCLASS IIStellaris PC w/ Laser, BL14304 The responsible firm name recalledBausch & LombDevice Malfunction21 states
DeviceCLASS IIStellaris PC w/ Laser Upgrade BL1433 (Stellaris PC w v3 recalledBausch & LombDevice Malfunction21 states
DeviceCLASS IIStellaris PC w/ Laser Upgrade BL14334 (Stellaris PC w v4 recalledBausch & LombDevice Malfunction21 states
DrugCLASS IIMuro 128 (sodium chloride) hypertonicity ophthalmic ointment recalledMuro 128Bausch & LombPackaging DefectsNationwide
DrugCLASS IISodium Chloride Hypertonicity Ophthalmic Ointment, 5% tube recalledBausch & LombOtherNationwide
DeviceCLASS IIBausch + Lomb Stellaris PC Vision Enhancement System recalledBausch & LombOtherNY
DrugCLASS IIMurocel (methylcellulose) Lubricant Opthalmic Solution (USP, 1%) recalledBausch & LombSterilityNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.