---
title: "AbbVie Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search AbbVie Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/abbvie-inc/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# AbbVie Inc. recall records

**4** reported ongoing

4 records in this archive. Latest source date May 18, 2026.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## Records and reported status

May 18, 2026 FDA drug enforcement

### [PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie company, North Chicago, IL 60064, Product of France, NDC 11...](https://isitonrecall.com/recall/fda-drug-d-0551-2026-pred-mild-prednisolone-acetate-ophthalmic-suspension-usp-0-12-10-ml-sterile-rx-only-allergen-inc-an/)

Failed Stability Specifications

Class III Reported ongoing

Distribution: US Nationwide.

[Official source for PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Aller...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0551-2026%22)

Sep 16, 2024 FDA drug enforcement

### [Refresh P.M., (Mineral Oil 42.5%, White Petrolatum 57.3%) Lubricant Eye Ointment, Net wt, 0.12 oz (3.5g) Tube, Distributed by: Allergen, an AbbVie company, Madison, NJ 07940, UP...](https://isitonrecall.com/recall/fda-drug-d-0664-2024-refresh-p-m-mineral-oil-42-5-white-petrolatum-57-3-lubricant-eye-ointment-net-wt-0-12-oz-3-5g-tube-d/)

Lack of Assurance of Sterility: The impacted lots may contain a breach in the tube seal.

Class II Reported ongoing

Distribution: Nationwide in the USA, Foreign Consignees (Austrailia, Canada, Great Britain)

[Official source for Refresh P.M., (Mineral Oil 42.5%, White Petrolatum 57.3%) Lubricant Eye Ointment, Net wt, 0.12 oz...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0664-2024%22)

Sep 16, 2024 FDA drug enforcement

### [Refresh LACRI-LUBE, (42.5% Mineral Oil, 57.3% White Petrolatum) Lubricant Eye Ointment, Net wt, 0.12 oz (3.5g) Tube, Distributed by: Allergen, an AbbVie company, Madison, NJ 079...](https://isitonrecall.com/recall/fda-drug-d-0665-2024-refresh-lacri-lube-42-5-mineral-oil-57-3-white-petrolatum-lubricant-eye-ointment-net-wt-0-12-oz-3-5g/)

Lack of Assurance of Sterility: The impacted lots may contain a breach in the tube seal.

Class II Reported ongoing

Distribution: Nationwide in the USA, Foreign Consignees (Austrailia, Canada, Great Britain)

[Official source for Refresh LACRI-LUBE, (42.5% Mineral Oil, 57.3% White Petrolatum) Lubricant Eye Ointment, Net wt, 0...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0665-2024%22)

Oct 17, 2023 FDA drug enforcement

### [Synthroid, Levothyroxine Sodium Tablets, USP 125mcg (0.125mg), 100-count bottle, Rx Only AbbVie Inc. North Chicago, IL 60064, U.S.A. NDC 0074-7068-11](https://isitonrecall.com/recall/fda-drug-d-0088-2024-synthroid-levothyroxine-sodium-tablets-usp-125mcg-0-125mg-100-count-bottle-rx-only-abbvie-inc-north/)

Labeling: Wrong Barcode- One (1) of every forty (40) unit dose blister will contain incorrect barcode information that causes a 125mcg unit dose is scanned as 200mcg unit dose.

Class III Reported ongoing

Distribution: Distributed in the US. No government or foreign consignees.

[Official source for Synthroid, Levothyroxine Sodium Tablets, USP 125mcg (0.125mg), 100-count bottle, Rx Only AbbVie I...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0088-2024%22)

## Reasons in these listed records

- Failed Stability Specifications
- Lack of Assurance of Sterility: The impacted lots may contain a breach in the tube seal.
- Labeling: Wrong Barcode- One (1) of every forty (40) unit dose blister will contain incorrect barcode information that causes a 125mcg unit dose is scanned as 200mcg unit dose.

These examples come from this result page and are not a ranking of every recall reason.

## Checking AbbVie Inc.

### Is there a recall on abbvie inc. right now?

This archive contains 4 records, including 4 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search AbbVie Inc.](https://isitonrecall.com/check/?q=AbbVie%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
