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Allergan Sales Recalls
14 recalls on record · September 30, 2015 to May 8, 2024 · Drugs, Medical Devices
Recalls by year
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17
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24
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 8, 2024Medical DevicesFDA
Allergan Sales, LLC recalls Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,
Hazard: Their is a potential that breast implants lack the lubricious coating that allows them to slide through the funnels during the implantation procedure.
April 3, 2019DrugsFDA
Allergan Sales, LLC recalls Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5% 5 mL bottles, Rx only, Allergan, Inc. Irv
Hazard: cGMP Deviations
November 22, 2017DrugsFDA
Allergan Sales, LLC recalls Lumigan (bimatoprost ophthalmic solution) 0.01%, 2.5 mL bottle, Rx only, Allergan, Irvine, CA 92612. NDC# 0023-3205-03
Hazard: Failed Impurities/Degradation Specifications.
November 22, 2017DrugsFDA
Allergan Sales, LLC recalls Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5%, Rx only, packaged in a) 2.5 mL NDC# 0023-
Hazard: Failed Impurities/Degradation Specifications.
July 5, 2017DrugsFDA
Allergan Sales, LLC recalls Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10%/0.2% sterile, 3.5 g tube, RX onl
Hazard: Failed Impurities/Degradation Specifications: stability testing results did not meet the specification for impurities.
April 19, 2017DrugsFDA
Allergan Sales, LLC recalls Lumigan (bimatoprost ophthalmic solution) 0.01%, 7.5 mL bottle, Rx only, Allergan Irvine, CA 92612, NDC 0023-3205-08.
Hazard: Failed Impurities/Degradation Specifications
October 19, 2016DrugsFDA
Allergan Sales, LLC recalls TAZORAC (tazarotene) Gel 0.05%, Rx only, packaged in 15 x 3.5 g professional sample containers, Manufactured by: Allerga
Hazard: Failed Content Uniformity Specifications
October 19, 2016DrugsFDA
Allergan Sales, LLC recalls TAZORAC (tazarotene) Gel 0.05%, Rx only, For Dermatologic Use Only, Not for Ophthalmic Use, packaged in a) 30 g tubes (N
Hazard: Failed Content Uniformity Specifications
July 13, 2016DrugsFDA
Allergan Sales, LLC recalls Tazorac (tazarotene) Gel 0.05%, 15 x 3.5g, sample packs, Allergan Inc, Irvine, CA 92612. UPC 300238335159
Hazard: Failed Content Uniformity Specifications.
July 13, 2016DrugsFDA
Allergan Sales, LLC recalls Tazorac (tazarotene) Gel 0.05%, Rx only, packaged in a) 30g (NDC 0023-8335-03) and b) 100g (NDC 0023-8335-10) tubes, All
Hazard: Failed Content Uniformity Specifications.
September 30, 2015DrugsFDA
Allergan Sales, LLC recalls BLEPHAMIDE (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10 %/0.2 %, 3.5 g tube, Rx only, ALL
Hazard: Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.
September 30, 2015DrugsFDA
Allergan Sales, LLC recalls FML (fluorometholone ophthalmic ointment) 0.1%, 3.5 g tube, Rx only, Allergan, Inc., Irvine, CA 92612, NDC 0023-0316-04
Hazard: Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.
September 30, 2015DrugsFDA
Allergan Sales, LLC recalls Refresh P.M. (Mineral Oil 42.5% and White Petrolatum 57.3%) Lubricant Eye Ointment, Net wt. 0.12 oz (3.5 g) tube, Allerg
Hazard: Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.
September 30, 2015DrugsFDA
Allergan Sales, LLC recalls Refresh Lacri-Lube (Mineral Oil 42.5% and White Petrolatum 56.8%) Lubricant Eye Ointment, packaged in a) Net wt. 0.12 oz
Hazard: Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.