Allergan, PLC. recalls
Every recall we track for Allergan, PLC. — 26 in all, from 2018–2020 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Allergan, PLC. peaked in 2019 (20); 26 since 2017. 4% rated “stop using now”.
All FDA recall records for Allergan, PLC. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 1 | 0 | 1 | 2 |
| 2019 | 1 | 11 | 7 | 1 | 20 |
| 2020 | 0 | 0 | 4 | 0 | 4 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Allergan, PLC. recalls
What to do if you have a recalled Allergan, PLC. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Allergan, PLC. recalls
8 shown- Lower riskDrug
Allergan, PLC. recalls Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz (10 mL) Sterile Distributed by: Allergan, an AbbVie
Allergan recalls Refresh Relieva PF Preservative-Free Lubricant Eye Drops due to missing instructions for use. Consumers should check product labels for lot numbers and expiration dates.
AllerganDec 30, 2020 - Lower riskMedical device
Allergan PLC recalls REFRESH CONTACTS¿ Contact Lens Comfort Drops 0.4 fl oz (12 mL) Sterile
Allergan recalls REFRESH Contact Lens Comfort Drops 0.4 fl oz due to missing instruction manual. Consumers should check product details and contact Allergan for guidance.
AllerganDec 29, 2020 - Lower riskDrug
Allergan PLC recalls Skin Medica Acne System, Contains: Purifying Foaming Wash (Salicylic Acid 2.0%), 5 fl oz.; Purifying Toner (Salicylic
Allergan recalls Skin Medica Acne System products that failed drug assay tests at 12 and 24 months, potentially containing insufficient salicylic acid and benzoyl peroxide.
AllerganJul 6, 2020 - Lower riskMedical device
Allergan PLC recalls Natrelle Silicone Filled Breast Implants for the following Styles and Sizes: Style 10, Style 15, Style 20, Style 40,
Allergan, PLC. - Allergan
Allergan, PLC.Nov 6, 2019 - Lower riskMedical device
Allergan PLC recalls XEN Gel Stent, REF 5513-001(US Model), Sterile, RX Only, (01)10888628032439 ; Other Model Numbers: 5507-001(Global
Allergan recalls XEN Gel Stents with specific lot numbers due to potential residual polishing compounds on the injector needle that could cause eye irritation, inflammation, or allergic reactions during glaucoma treatment.
AllerganOct 30, 2019 - Use cautionMedical device
Allergan PLC recalls Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:
Allergan recalls specific saline-filled breast implants due to higher risk of anaplastic large cell lymphoma (BIA-ALCL) in patients with textured implants.
AllerganJul 24, 2019 - Use cautionDrug
Allergan, PLC. recalls OZURDEX (dexamethasone intravitreal implant) 0.7 mg), 1 single-use plastic applicator contained within carton, Rx only,
Allergan recalls OZURDEX 0.7 mg intravitreal implants (NDC 0023-3348-07) after finding silicone particles during manufacturing. This may cause eye injury. Consumers should contact Allergan for details.
AllerganDec 20, 2018 - UnratedDrug
Allergan, PLC. recalls Allergan Taytulla Softgel Capsules, 1 mg/20 mcg, 6x28 blister card Physicians's Sample - Not for Sale Distributed by:
Allergan recalls physicians' sample Taytulla Softgel Capsules due to contraceptive tablets being out of sequence. This may cause unintended pregnancy. Contact Allergan for details.
AllerganMay 24, 2018
Allergan, PLC. recall questions
How many recalls has Allergan, PLC. had?
26 recalls from Allergan, PLC. are on record with U.S. safety agencies, from 2018–2020 (21 medical device, 5 drug).
What is the most recent Allergan, PLC. recall?
Allergan, PLC. recalls Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz (10 mL) Sterile Distributed by: Allergan, an AbbVie, dated Dec 30, 2020. Every Allergan, PLC. recall is listed on this page, newest first.
Why are Allergan, PLC. products recalled?
The most common reasons on record: SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints. (2).
What should I do if I have a recalled Allergan, PLC. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Allergan, PLC. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.