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VIRTUS PHARMACEUTICALS OPCO II L

VIRTUS PHARMACEUTICALS OPCO II L Recalls

All product recalls associated with VIRTUS PHARMACEUTICALS OPCO II L.

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Recall Summary

Total Recalls

597

Past Year

Class I (Serious)

Most Recent

May 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 361–380 of 597 recalls

Hyoscyamine Disintegrating Tablets (Virtus) – Potency Variation (2016)

Failed Content Uniformity Specifications: resulting in both superpotent and subpotent tablets.

Class IHigh

FDASep 2, 2016Nationwide• VIRTUS PHARMACEUTICALS OPCO II L

Hyoscyamine Tablets (Virtus) – Potency Variation (2016)

Failed Content Uniformity Specifications: resulting in both superpotent and subpotent tablets.

Class IHigh

FDASep 2, 2016Nationwide• VIRTUS PHARMACEUTICALS OPCO II L

Amoxicillin Suspension (West-Ward) – Missing Label Panel (2016)

Labeling: Label Error on Declared Strength- bottles missing colored coded panel where strength of the product is displayed.

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Class III

Low

FDAAug 18, 2016Nationwide• West-Ward Pharmaceuticals Corp.

Kohler Portable Generators (Sumec) – Electrical Shock Risk (2016)

This recall involves the following Kohler portable generator models: PRO3.7, PRO3.7E, PRO5.2, PRO5.2E, and GEN5.0 with Spec Number PA-GEN50-3003. These generators have black frame assemblies and blue fuel tanks. The PRO3.7, PRO5.2 and GEN5.0 models have manual recoil start. The PRO3.7E and PRO5.2E have both manual recoil and electric start. Only generators with serial number 4528733735 or lower, and a manufacture date prior to 06 2016, representing the months and year of manufacture, are included in this recall. Model numbers, serial numbers, spec number and manufacturing date codes are on a silver label placed on each generator on the lower black frame assemblies.

CPSCAug 9, 2016Nationwide• Sumec Machinery & Electric Co. Ltd., of China

Cranberry Tablets (Reese Pharmaceutical) – Undeclared Calcium (2016)

The finished product label on the Cranberry supplement does not include Calcium. Users of the product may be unaware of the Calcium in the supplement. Additionally the amount per serving as written on the product label is incorrect and should be 500mg, not 900mg.

Class IIILow

FDAAug 2, 2016AL, AZ, CA +16 more• Reese Pharmaceutical Company

Papaverine/Phentolamine Vials (Vital Care Compounder) – Sterility Concern (2016)

Lack of Assurance of Sterility

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VIRTUS PHARMACEUTICALS OPCO II L Recalls

Recall Summary

Hyoscyamine Disintegrating Tablets (Virtus) – Potency Variation (2016)

Hyoscyamine Tablets (Virtus) – Potency Variation (2016)

Amoxicillin Suspension (West-Ward) – Missing Label Panel (2016)

Kohler Portable Generators (Sumec) – Electrical Shock Risk (2016)

Cranberry Tablets (Reese Pharmaceutical) – Undeclared Calcium (2016)

Papaverine/Phentolamine Vials (Vital Care Compounder) – Sterility Concern (2016)

Papaverine/Phentolamine/Prostaglandin (Vital Care Compounder) – Sterility Issue (2016)

Brilliant Blue G 0.025% (Vital Care Compounder) – Sterility Uncertainty (2016)

C-PAP/PHEN/PROST/Atrop (Vital Care) – Sterility Risk (2016)

Pre-Op Pledget Solution (Vital Care) – Sterility Risk (2016)

Moxifloxacin/Dexamethazone 0.5%/0.1% (Vital Care Compounder) – Sterility Risk (2016)

Morphine Sulfate Injection (Vital Care) – Sterility Concern (2016)

Hydroxyzine HCl Injection (Vital Care) – Sterility Concern (2016)

DMSO with Lidocaine (Vital Care) – Sterility Concern (2016)

Hyaluronidase (Vital Care) – Sterility Risk (2016)

C-PAP/PHEN/PROST/ATROP Injection (Vital Care Compounder) – Sterility Problem (2016)

Apomorphine HCl Injection (Vital Care) – Sterility Risk (2016)

MOXI/DEX/KETOROLAC 0.5%/0.1%/0.4% (Vital Care Compounder) – Sterility Issue (2016)

Methylcobalamin (Vital Care) – Sterility Risk (2016)

Autologous Serum Tears (Vital Care) – Sterility Risk (2016)