ALLERGAN recalls
Every recall we track for ALLERGAN — 4 in all, from 2017–2018 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for ALLERGAN 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 | 2 | 0 | 2 |
| 2018 | 0 | 1 | 1 | 0 | 2 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 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 |
What to do if you have a recalled ALLERGAN product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All ALLERGAN recalls
4 shown- Lower riskDrug
ALLERGAN recalls INFed (Iron Dextran Injection USP) 100 mg elemental iron/2 mL (50 mg/mL), Rx only, packaged in 2 mL Sterile Single Dose
Allergan recalls INFed (Iron Dextran Injection USP) 100 mg elemental iron/2 mL (50 mg/mL) due to failed stability tests. This medication, prescribed only, may have incorrect iron levels.
AllerganNov 8, 2018 - Use cautionDrug
ALLERGAN recalls NORCO (Hydrocodone Bitartrate and Acetaminophen) Tablets, USP, 10 mg/325 mg, 100-count bottles, Rx Only, Distributed
Allergan recalls specific lots of NORCO 10 mg/325 mg tablets because the primary label is missing the required CII controlled drug classification.
AllerganFeb 2, 2018 - Lower riskDrug
ALLERGAN recalls INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL), Rx Only, packaged in a) single dose vials,
Allergan recalls INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml vials due to failed stability testing for iron content. This affects certain lots manufactured by Patheon Italia S.p.A. in Italy.
AllerganDec 13, 2017 - Lower riskDrug
ALLERGAN recalls Viokace (pancrelipase) tablets, 20,880 USP units, 100-count bottle, Rx only, Distributed by; Allergan USA Inc., Irvine,
Allergan recalls 100-count Viokace tablets (NDC 58914-117-10) due to subpotent drug stability issues. This affects prescription-only enzyme supplements for pancreatic enzyme replacement.
AllerganDec 4, 2017
ALLERGAN recall questions
How many recalls has ALLERGAN had?
4 recalls from ALLERGAN are on record with U.S. safety agencies, from 2017–2018.
What is the most recent ALLERGAN recall?
ALLERGAN recalls INFed (Iron Dextran Injection USP) 100 mg elemental iron/2 mL (50 mg/mL), Rx only, packaged in 2 mL Sterile Single Dose, dated Nov 8, 2018. Every ALLERGAN recall is listed on this page, newest first.
What should I do if I have a recalled ALLERGAN product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new ALLERGAN 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.