Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

362 recalls · Class III, newest first

Class III · Low risk

Tobramycin Ophthalmic Oint.

Labeling: Label Mix-up: The affected units were labeled incorrectly describing the product as "ointment" instead of "solution."

Terminated Labeling / mix-up Stat Rx USA NDC 16590-224-05 D-050-2013
Class III · Low risk

Pitocin (Oxytocin Injection, USP)

Labeling: Label Mix-up: Pitocin storage conditions should be labeled, "Store between 20¿ to 25¿C (68¿ to 77¿F)". Pitocin lot 225867 and part of Pitocin lot 231423 were labeled, "Store between 20¿ to 25¿C (28¿ to 77¿F)".

Terminated Labeling / mix-up JHP Pharmaceuticals, LLC NDC 42023-116-02 D-1420-2012
Class III · Low risk

Midol Complete

Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of capsules/caplets that should be taken within a 24-hour period, does not match the statement on the carton.

Terminated Labeling / mix-up Bayer Healthcare, LLC NDC 0280-8005-16 D-1424-2012
Class III · Low risk

Midol Complete

Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of capsules/caplets that should be taken within a 24-hour period, does not match the statement on the carton.

Terminated Labeling / mix-up Bayer Healthcare, LLC NDC 0280-8015-24 D-1423-2012
Class III · Low risk

Loxitane Capsules

Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.

Terminated Labeling / mix-up Watson Laboratories Inc NDC 52544-495-01 D-1403-2012
Class III · Low risk

Loxapine Capsules USP

Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.

Terminated Labeling / mix-up Watson Laboratories Inc NDC 0591-0372-01 D-1402-2012
Class III · Low risk

Loxapine Capsules USP

Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.

Terminated Labeling / mix-up Watson Laboratories Inc NDC 0591-0371-01 D-1401-2012
Class III · Low risk

Loxapine Capsules USP

Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.

Terminated Labeling / mix-up Watson Laboratories Inc NDC 0591-0370-01 D-1400-2012
Class III · Low risk

Loxapine Capsules USP

Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.

Terminated Labeling / mix-up Watson Laboratories Inc NDC 00591-0369-01 D-1399-2012
Class III · Low risk

Ciprofloxacin Tablets

Labeling Illegible: Missing Label; The voluntary recall of the aforementioned batch of product is being initiated due to two bottles missing container labels.

Terminated Labeling / mix-up Pack Pharmaceuticals NDC 16571-412-10 D-1422-2012
Class III · Low risk

Metoclopramide Oral Solution

Labeling: Correct Labeled Product Miscart/Mispack: The shipper label displayed "5 mL x 50," instead of "10 mL x 50,"

Terminated Labeling / mix-up VistaPharm, Inc. D-1669-2012

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