Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II drug recalls - moderate risk

Class II means the product may cause temporary or medically reversible harm, and serious harm is unlikely. It is by far the largest recall class - most potency, dissolution and labeling problems land here.

14,535 recalls, newest first.

Class II · Moderate risk

Meprobamate

Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is recalling meprobamate because an out of specification result for an impurity diphenyl sulfone .

Terminated Impurity / degradation Watson Laboratories Inc NDC 0591-5238-01 D-204-2013
Class II · Moderate risk

Meprobamate

Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is recalling meprobamate because an out of specification result for an impurity diphenyl sulfone .

Terminated Impurity / degradation Watson Laboratories Inc NDC 9591-5239-01 D-203-2013
Class II · Moderate risk

Ciprofloxacin Tablets USP

Presence of Foreign Substance(s): A complaint was received for a rubber-like material in a 500 mg Ciprofloxacin tablet.

Terminated Particulate / foreign matter West-ward Pharmaceutical Corp. NDC 0143-9928-01 D-220-2013
Class II · Moderate risk

Benjamins Infants Gripe Mixture

CGMP Deviations: this product is being recalled because an FDA inspection revealed that it was not manufactured under current good manufacturing practices.

Terminated cGMP deviation Carib Import & Export, Inc. D-307-2013
Class II · Moderate risk

Daytrana (methylphenidate)

Defective Delivery System: Out of Specification (OOS) results for the z-statistic value, which relates to the patients and caregiver ability to remove the release liner from the patch adhesive prior to administration, were obtained.

Terminated Packaging defect Noven Pharmaceuticals, Inc. NDC 68968-5552-3 D-312-2013
Class II · Moderate risk

ZoDen PD

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-0073-16 D-546-2013
Class II · Moderate risk

ZoDen DM Drops

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-0080-30 D-545-2013
Class II · Moderate risk

Z-Dex Syrup

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-0002-16 D-544-2013
Class II · Moderate risk

Trigofen DM Drops

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-0082-30 D-542-2013
Class II · Moderate risk

Trigofen Drops

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-0081-30 D-541-2013
Class II · Moderate risk

Tri-Dex PE

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-088-16 D-540-2013
Class II · Moderate risk

TL-Hist PD Drops

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-083-30 D-539-2013
Class II · Moderate risk

TL Hist DM

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-068-16 D-538-2013
Class II · Moderate risk

Tl-Dex Dm

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-067-16 D-537-2013
Class II · Moderate risk

Mesehist WC

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-0075-16 D-536-2013
Class II · Moderate risk

Mesehist DM

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-0085-16 D-535-2013
Class II · Moderate risk

CPM / PSE DM Drops

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-072-30 D-534-2013
Class II · Moderate risk

CPM / PSE Drops

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 13811-071-30 D-533-2013
Class II · Moderate risk

Poly-Vent IR

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 50991-561-60 D-531-2013
Class II · Moderate risk

Poly-Vent DM Tablets

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 50991-309-60 D-530-2013
Class II · Moderate risk

Poly Hist Forte

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 50991-210-01 D-529-2013
Class II · Moderate risk

Lusair Liquid

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

Terminated Wrong potency / content TG United, Inc. NDC 23359-017-16 D-528-2013

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