Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Labeling errors & mix-ups

Wrong label, wrong strength, mixed-up products, or packaging errors. One of the most dangerous causes - you can end up taking the wrong drug or the wrong dose.

1,411 FDA drug recalls with this cause, newest first.

This is exactly what it sounds like: the wrong label on the right product, the wrong strength printed on the bottle, a missing or illegible lot number and expiry date, or two products mixed up during packaging. It is dangerous precisely because the pill or liquid itself may be fine, yet the patient has no way of knowing what they are actually taking. A high share of the Class I recalls in this group are mix-ups where a stronger product ended up in a weaker product's packaging.

Class II · Moderate risk

Aripiprazole Tablets

Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had aripiprazole 5 mg tablets, 100 count.

Terminated Labeling / mix-up Alembic Pharmaceuticals Limited NDC 62332-097-30 D-1341-2020
Class II · Moderate risk

Gaviscon Liquid Antacid Extra Strength

Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.

Terminated Labeling / mix-up Glaxosmithkline Consumer Healthcare Holdings NDC 0135-0095-41 D-1325-2020
Class II · Moderate risk

Lisinopril Tablets

Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.

Terminated Labeling / mix-up Lupin Pharmaceuticals Inc. NDC 68180-513-03 D-1290-2020
Class II · Moderate risk

Lisinopril Tablets USP

Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril tablets inside of 2 sealed bottles of 20 mg/1000 count bottles.

Terminated Labeling / mix-up Lupin Pharmaceuticals Inc. NDC 68180-0981-03 D-1250-2020
Class II · Moderate risk

Advil Liqui-Gel Mini 160+20+20 CT

Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.

Terminated Labeling / mix-up Glaxosmithkline Consumer Healthcare Holdings NDC 0573-1715-59 D-1069-2020
Class III · Low risk

PrediniSONE Tablets

Labeling: Incorrect or Missing Exp Date - An incorrect expiration date has been identified on Prednisone Tablets USP 5 mg

Terminated Labeling / mix-up Par Pharmaceutical Inc. NDC 0603-5337-31 D-1035-2020
Class III · Low risk

Quetiapine Fumarate Extended-Release Tablets

Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.

Terminated Labeling / mix-up The Harvard Drug Group D-1002-2020
Class III · Low risk

Quetiapine Fumarate Extended-Release Tablets

Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.

Terminated Labeling / mix-up The Harvard Drug Group D-1001-2020
Class III · Low risk

Quetiapine Fumarate Extended-Release Tablets

Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.

Terminated Labeling / mix-up The Harvard Drug Group D-1000-2020
Class III · Low risk

Quetiapine Fumarate Extended-Release Tablets

Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.

Terminated Labeling / mix-up The Harvard Drug Group D-0999-2020
Class III · Low risk

Discount Drug Mart

Labeling: Incorrect or Missing Lot and/or Expiration date.

Terminated Labeling / mix-up AAA Pharmaceutical, Inc. NDC 53943-192-04 D-0868-2020
Class III · Low risk

TRAMADOL HYDROCHLORIDE Tablets

Labeling: Incorrect package insert - Patient leaflets for the specified lots of unscored tablets contain language relative to a 25 mg dosing titration that necessitates the use of a scored 50 mg tablet.

Terminated Labeling / mix-up Golden State Medical Supply Inc. NDC 60429-588-01 D-0856-2020